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Ew0zFtKLlZmvWycu | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | The rate law for a reaction between the substances A and B is given by Rate = k[A]<sup>n</sup> [B]<sup>m</sup> On doubling the concentration of A and halving the concentration of B, the ratio of the new rate to the earlier rate of the reaction will be as | [{"identifier": "A", "content": "(m + n)"}, {"identifier": "B", "content": "(n - m) "}, {"identifier": "C", "content": "2<sup>( n - m)</sup>"}, {"identifier": "D", "content": "$${1 \\over {{2^{(m + n)}}}}$$ "}] | ["C"] | null | $$Rat{e_1} = k{\left[ A \right]^n}{\left[ B \right]^m};$$
<br><br>$$Rat{e_2} = k{\left[ {2A} \right]^n}{\left[ {{\raise0.5ex\hbox{$\scriptstyle 1$}
\kern-0.1em/\kern-0.15em
\lower0.25ex\hbox{$\scriptstyle 2$}}B} \right]^m}$$
<br><br>$$\therefore$$ $$\,\,\,\,{{Rat{e_2}} \over {Rat{e_1}}} = {{k{{\left[ {2A} \right]}^n}{... | mcq | aieee-2003 | 1,234 |
s2ZXsTcGrJPXu1R4 | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | The rate equation for the reaction 2A + B $$\to$$ C is found to be: rate k[A][B]. The correct
statement in relation to this reaction is that the | [{"identifier": "A", "content": "unit of K must be s<sup>-1</sup>"}, {"identifier": "B", "content": "values of k is independent of the initial concentration of A and B"}, {"identifier": "C", "content": "rate of formation of C is twice the rate of disappearance of A "}, {"identifier": "D", "content": "t<sub>1/2</sub> is... | ["B"] | null | The velocity constant depends on temperature only. It is independent of concentration of reactants. | mcq | aieee-2004 | 1,235 |
NXeuAeEwemgjHCld | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | For the non – stoichiometre reaction 2A + B $$\to$$ C + D, the following kinetic data were obtained in three
separate experiments, all at 298 K.
<div style="overflow-x: auto">
<style type="text/css">
.tg {border-collapse:collapse;border-spacing:0;}
.tg td{font-family:Arial, sans-serif;font-size:14px;padding:10px 5px;b... | [{"identifier": "A", "content": "$${{dc} \\over {dt}} = k[A]{[B]^2}$$ "}, {"identifier": "B", "content": "$${{dc} \\over {dt}} = k[A]$$ "}, {"identifier": "C", "content": "$${{dc} \\over {dt}} = k[A]{[B]}$$"}, {"identifier": "D", "content": "$${{dc} \\over {dt}} = k[A^2]{[B]}$$ "}] | ["B"] | null | Let rate of reaction $$ = {{d\left[ C \right]} \over t} = k{\left[ A \right]^x}{\left[ B \right]^y}$$
<br><br>Now from the given data
<br><br>$$1.2 \times {10^{ - 3}} = k{\left[ {0.1} \right]^x}{\left[ {0.1} \right]^y}\,\,\,\,\,...\left( i \right)$$
<br><br>$$1.2 \times {10^{ - 3}} = k{\left[ {0.1} \right]^x}{\left[ {0... | mcq | jee-main-2014-offline | 1,238 |
9ZokgutcPux9fYlMYPzm1 | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | The rate law for the reaction below is given by the expression k [A] [B]
<br/><br/>A + B $$ \to $$ Product
<br/><br/>If the concentration of B is increased from 0.1 to 0.3 mole, keeping the value of A at 0.1 mole, the rate constant will be :
| [{"identifier": "A", "content": "k"}, {"identifier": "B", "content": "k/3"}, {"identifier": "C", "content": "3k"}, {"identifier": "D", "content": "9k"}] | ["A"] | null | Rate constant only depends on temperature only and it is independed of concentration of reactants. | mcq | jee-main-2016-online-10th-april-morning-slot | 1,240 |
JjOycwZJFaC09V6aDBqoQ | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | For a reaction consider the plot of $$\ell $$n k versus 1/T given in the figure. If the rate constant of this reaction at 400 K is 10<sup>–5</sup> s<sup>–1</sup>, then the rate constant at 500 K is –
<br/><br/><img src="data:image/png;base64,UklGRmoLAABXRUJQVlA4IF4LAACwhQCdASrFAqQBP4HA3mW2Mi6nIVeI2sAwCWlu4XYBG/Pt8of4b... | [{"identifier": "A", "content": "10<sup>$$-$$4</sup> s<sup>$$-$$1</sup>"}, {"identifier": "B", "content": "4 $$ \\times $$ 10<sup>$$-$$4</sup> s<sup>$$-$$1</sup>"}, {"identifier": "C", "content": "10<sup>$$-$$6</sup> s<sup>$$-$$1</sup>"}, {"identifier": "D", "content": "2 $$ \\times $$ 10<sup>$$-$$4</sup> s<sup>$$-$$1<... | ["A"] | null | From Arhenius equation,
<br><br>K = Ae$$^{ - {{Ea} \over {RT}}}$$
<br><br>taking log both sides,
<br><br>lnk = lnA $$-$$ $${{{Ea} \over {RT}}}$$
<br><br>So in lnK vs $${1 \over T}$$ graph
<br><br>slope = $$-$$ $${{{Ea} \over R}}$$
<br><br>Rate constant at 400 K is = 10<sup>$$-$$5</sup> s<sup>$$-$$1</sup>
<br><br>Let r... | mcq | jee-main-2019-online-12th-january-evening-slot | 1,241 |
Sda0nfjcRYSDjjEV8p9xO | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | For the reaction 2A + B $$ \to $$ C, the values of initial rate at diffrent reactant concentrations are
given in the table below. The rate law for the reaction is :
<br/><br/><style type="text/css">
.tg {border-collapse:collapse;border-spacing:0;}
.tg td{font-family:Arial, sans-serif;font-size:14px;padding:10px 5px;bo... | [{"identifier": "A", "content": "Rate = k[A][B]<sup>2</sup>"}, {"identifier": "B", "content": "Rate = k[A]<sup>2</sup>[B]<sup>2</sup>"}, {"identifier": "C", "content": "Rate = k[A]<sup>2</sup>[B]"}, {"identifier": "D", "content": "Rate = k[A][B]"}] | ["A"] | null | Rate law for the reaction,
<br><br>2A + B $$ \to $$ C
<br><br>Rate law (R) = k[A]<sup>x</sup>[B]<sup>y</sup>
<br><br>From experiment 1 :
<br><br>R<sub>1</sub> = 0.045 = k[0.05]<sup>x</sup> [0.05]<sup>y</sup> ............(i)
<br><br>From experiment 2 :
<br><br>R<sub>2</sub> = 0.090 = k[0.1]<sup>x</sup> [0.05]<sup>y</sup... | mcq | jee-main-2019-online-8th-april-morning-slot | 1,242 |
77MBz4uXb4bQpusHe22VA | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | The following results were obtained during kinetic studies of the reaction ;
<br/><br/>2A + B $$ \to $$ Products
<br/><br/><style type="text/css">
.tg {border-collapse:collapse;border-spacing:0;}
.tg td{font-family:Arial, sans-serif;font-size:14px;padding:10px 5px;border-style:solid;border-width:1px;overflow:hidden;w... | [{"identifier": "A", "content": "5"}, {"identifier": "B", "content": "10"}, {"identifier": "C", "content": "1"}, {"identifier": "D", "content": "100"}] | ["B"] | null | <p>To determine the time required to consume half of A, we must first determine the rate law for the reaction based on the provided kinetic data.</p>
<p>From the data, we can write the general rate law for the reaction as:</p>
<p>$$ \text{Rate} = k [A]^m [B]^n $$</p>
<p>We can now use the experimental data to find t... | mcq | jee-main-2019-online-9th-january-morning-slot | 1,243 |
1krz07z5u | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | For a reaction of order n, the unit of the rate constant is : | [{"identifier": "A", "content": "mol<sup>1$$-$$n</sup> L<sup>1$$-$$n</sup> s"}, {"identifier": "B", "content": "mol<sup>1$$-$$n</sup> L<sup>2n</sup> s<sup>$$-$$1</sup>"}, {"identifier": "C", "content": "mol<sup>1$$-$$n</sup> L<sup>n$$-$$1</sup> s<sup>$$-$$1</sup>"}, {"identifier": "D", "content": "mol<sup>1$$-$$n</sup>... | ["C"] | null | Rate = k[A]<sup>n</sup><br><br>comparing units<br><br>$${{(mol/l)} \over {\sec }} = k{\left( {{{mol} \over l}} \right)^n}$$<br><br>$$ \Rightarrow k = mo{l^{(l - n)}}{l^{(n - 1)}}{s^{ - 1}}$$ | mcq | jee-main-2021-online-27th-july-morning-shift | 1,245 |
1ldpqcpkw | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | <p>A $$\to$$ B</p>
<p>The rate constants of the above reaction at 200 K and 300 K are 0.03 min$$^{-1}$$ and 0.05 min$$^{-1}$$ respectively. The activation energy for the reaction is ___________ J (Nearest integer)</p>
<p>(Given : $$\mathrm{ln10=2.3}$$</p>
<p>$$\mathrm{R=8.3~J~K^{-1}~mol^{-1}}$$
<p>$$\mathrm{\log5=0.70}... | [] | null | 2520 | $$
\begin{aligned}
& \log \frac{\mathrm{k}_2}{\mathrm{k}_1}=\frac{\mathrm{E}_{\mathrm{a}}}{2.3 \times 8.3}\left(\frac{1}{200}-\frac{1}{300}\right) \\\\
& \log \frac{0.05}{0.03}=\frac{E_a}{2.3 \times 8.3}\left(\frac{1}{600}\right) \\\\
& \begin{aligned}
(0.70-0.48)=\frac{E_a}{2.3 \times 8.3} \times \frac{1}{600}
\end{al... | integer | jee-main-2023-online-31st-january-morning-shift | 1,246 |
1ldyho7ej | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | <p>The number of correct statement/s from the following is __________</p>
<p>A. Larger the activation energy, smaller is the value of the rate constant.</p>
<p>B. The higher is the activation energy, higher is the value of the temperature coefficient.</p>
<p>C. At lower temperatures, increase in temperature causes more... | [] | null | 3 | (A) $k=A e^{-\frac{E_{a}}{R T}}\left(E_{a} \uparrow k \downarrow\right)$
<br><br>
(B) $\ln k=\ln A-\frac{E_{a}}{R T}$
<br><br>
$$
\frac{1}{\mathrm{k}} \cdot \frac{\mathrm{dk}}{\mathrm{dT}}=\frac{+\mathrm{E}_{\mathrm{a}}}{\mathrm{RT}^{2}}
$$
<br><br>
$\mathrm{E}_{\mathrm{a}} \uparrow$ temp. coefficient $\uparrow$<br><br... | integer | jee-main-2023-online-24th-january-morning-shift | 1,247 |
1lgysc9q2 | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | <p>The correct reaction profile diagram for a positive catalyst reaction.</p> | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1lgzoodm5/e9e3fe48-eb8d-4b56-97db-d30a64dd6aa9/03c949d0-e549-11ed-b775-8921c6ad38e2/file-1lgzoodm6.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1lgzoodm5/e9e3fe48-eb8d-4b56-97db-d30a64dd6aa9/03c... | ["D"] | null | Most of the chemical reactions have energy barrier.<br/><br/>
A positive catalyst in a chemical reaction increases the
rate of reaction by lowering the energy barrier. It does
not alter the energy of reactant as well as product. | mcq | jee-main-2023-online-8th-april-evening-shift | 1,248 |
lv3xm5t5 | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-laws-and-rate-constant | <p>For a reaction $$A \xrightarrow{\mathrm{K}_1} \mathrm{~B} \xrightarrow{\mathrm{K}_2} \mathrm{C}$$
If the rate of formation of B is set to be zero then the concentration of B is given by :</p> | [{"identifier": "A", "content": "$$(\\mathrm{K}_1-\\mathrm{K}_2)[\\mathrm{A}]$$\n"}, {"identifier": "B", "content": "$$(\\mathrm{K}_1+\\mathrm{K}_2)[\\mathrm{A}]$$\n"}, {"identifier": "C", "content": "$$\\mathrm{K}_1 \\mathrm{K}_2[\\mathrm{~A}]$$\n"}, {"identifier": "D", "content": "$$(\\mathrm{K}_1 / \\mathrm{K}_2)[\\... | ["D"] | null | <p>To determine the concentration of $ \mathrm{B} $ when the rate of formation of $ \mathrm{B} $ is set to zero, let's consider the reaction sequence:</p>
<p>$$ \mathrm{A} \xrightarrow{\mathrm{K}_1} \mathrm{B} \xrightarrow{\mathrm{K}_2} \mathrm{C} $$</p>
<p>The rate of formation of $ \mathrm{B} $ from $ \mathrm{A} $ ... | mcq | jee-main-2024-online-8th-april-evening-shift | 1,249 |
ZwNFCsTerSdJh5af | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | The differential rate law for the reaction H<sub>2</sub> + I<sub>2</sub> $$\to$$ 2HI is | [{"identifier": "A", "content": "$$ - {{d\\left[ {{H_2}} \\right]} \\over {dt}}$$ = $$ - {{d\\left[ {{I_2}} \\right]} \\over {dt}}$$ = $$ - {{d\\left[ {{HI}} \\right]} \\over {dt}}$$"}, {"identifier": "B", "content": "$$ {{d\\left[ {{H_2}} \\right]} \\over {dt}}$$ = $$ {{d\\left[ {{I_2}} \\right]} \\over {dt}}$$ = $$ {... | ["D"] | null | rate of appearance of $$HI = {1 \over 2}{{d\left[ {HI} \right]} \over {dt}}$$
<br><br>rate of formation of $${H_2} = {{ - d\left[ {{H_2}} \right]} \over {dt}}$$
<br><br>rate of formation of $${I_2} = {{ - d\left[ {{I_2}} \right]} \over {dt}}$$
<br><br>hence $${{ - d\left[ {{H_2}} \right]} \over {dt}} = - {{ - d\left... | mcq | aieee-2002 | 1,251 |
kMSXVWGi653VzsQd | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | For a reaction $${1 \over 2}A \to 2B$$ rate of disappearance of ‘A’ is related to the rate of appearance of ‘B’ by the
expression | [{"identifier": "A", "content": "$$ - {{d[A]} \\over {dt}}$$ = $${1 \\over 2}{{d[B]} \\over {dt}}$$"}, {"identifier": "B", "content": "$$ - {{d[A]} \\over {dt}}$$ = $${1 \\over 4}{{d[B]} \\over {dt}}$$"}, {"identifier": "C", "content": "$$ - {{d[A]} \\over {dt}}$$ = $${{d[B]} \\over {dt}}$$ "}, {"identifier": "D", "con... | ["B"] | null | The rates of reactions for the reaction
<br><br>$${1 \over 2}A \to 2B$$
<br><br>can be written either as
<br><br>$$ - 2{d \over {dt}}\left[ A \right]\,\,$$ with respect to $$'A'$$
<br><br>or $$\,\,\,\,\,$$ $${1 \over 2}{d \over {dt}}\left[ B \right]\,\,\,\,$$ with respect to $$'B'$$
<br><br>From the above, we have
<... | mcq | aieee-2008 | 1,252 |
Fee6Hpm0BqiHYc6y | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | The rate of a chemical reaction doubles for every 10<sup>o</sup>C rise of temperature. If the temperature is raised
by 50<sup>o</sup>C , the rate of the reaction increases by about : | [{"identifier": "A", "content": "24 times "}, {"identifier": "B", "content": "32 times"}, {"identifier": "C", "content": "64 times"}, {"identifier": "D", "content": "10 times "}] | ["B"] | null | Since for every $${10^ \circ }C$$ rise in temperature rate doubles for $${50^ \circ }C$$ rise in temp increase in reaction rate $$ = {2^5} = 32$$ times | mcq | aieee-2011 | 1,253 |
XBGUNKwE9hF2PnBg4THCA | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | For a reaction scheme $$A\buildrel {{k_1}} \over
\longrightarrow B\buildrel {{k_2}} \over
\longrightarrow C$$,
<br/><br/> if
the rate of formation of B is set to be zero then
the concentration of B is given by : | [{"identifier": "A", "content": "$${k_1}{k_2}[A]$$"}, {"identifier": "B", "content": "$$\\left( {{{{k_1}} \\over {{k_2}}}} \\right)[A]$$"}, {"identifier": "C", "content": "$$({k_1} + {k_2})[A]$$"}, {"identifier": "D", "content": "$$({k_1} - {k_2})[A]$$"}] | ["B"] | null | Given,
the rate of formation of B is set to be zero.
<br><br>$$ \therefore $$ $${{d\left[ B \right]} \over {dt}} = 0$$
<br><br>For this reaction,
<br><br>$$A\mathrel{\mathop{\kern0pt\longrightarrow}
\limits_{{R_1}}^{{k_1}}} B$$
<br><br>Rate of reaction for this reaction (R<sub>1</sub>) = $${k_1}\left[ A \right]$$
<br><... | mcq | jee-main-2019-online-8th-april-evening-slot | 1,255 |
y3VJgXGz1vuzitLKAm3rsa0w2w9jx54j4lu | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | In the following reaction; xA $$ \to $$ yB
<br/>$${\log _{10}}\left[ { - {{d\left[ A \right]} \over {dt}}} \right] = {\log _{10}}\left[ {{{d\left[ B \right]} \over {dt}}} \right] + 0.3010$$
<br/>'A' and 'B' respectively can be : | [{"identifier": "A", "content": "n-Butane and Iso-butane"}, {"identifier": "B", "content": "C<sub>2</sub>H<sub>4</sub> and C<sub>4</sub>H<sub>8</sub>"}, {"identifier": "C", "content": "C<sub>2</sub>H<sub>4</sub> and C<sub>6</sub>H<sub>6</sub>"}, {"identifier": "D", "content": "N<sub>2</sub>O<sub>4</sub> and NO<sub>2</s... | ["B"] | null | xA $$ \to $$ yB
<br><br>$${1 \over x}\left\{ { - {{d\left[ A \right]} \over {dt}}} \right\} = {1 \over y}\left\{ {{{d\left[ B \right]} \over {dt}}} \right\}$$
<br><br>$$ \Rightarrow $$ $$ - {{d\left[ A \right]} \over {dt}} = {x \over y}\left\{ {{{d\left[ B \right]} \over {dt}}} \right\}$$
<br><br>Taking log both sides,... | mcq | jee-main-2019-online-12th-april-morning-slot | 1,256 |
SAPfnXOxLl6aUoklKX3rsa0w2w9jx8xfted | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | NO<sub>2</sub> required for a reaction is produced by the decomposition of N<sub>2</sub>O<sub>5</sub> in CCl<sub>4</sub> as per the equation,
<br/>2N<sub>2</sub>O<sub>5</sub>(g) $$ \to $$ 4NO<sub>2</sub>(g) + O<sub>2</sub>(g).
<br/>The initial concentration of N<sub>2</sub>O<sub>5</sub> is 3.00 mol L<sup>–1</sup>
and ... | [{"identifier": "A", "content": "2.083 \u00d7 10<sup>\u20133</sup>\n mol L<sup>\u20131</sup>\n min<sup>\u20131</sup>"}, {"identifier": "B", "content": "8.333 \u00d7 10<sup>\u20133</sup>\n mol L<sup>\u20131</sup>\n min<sup>\u20131</sup>"}, {"identifier": "C", "content": "4.167 \u00d7 10<sup>\u20133</sup>\n mol L<sup>\u2... | ["D"] | null | Rate of disappearance of N<sub>2</sub>O<sub>5</sub> = $$ - {{\Delta \left[ {{N_2}{O_5}} \right]} \over {\Delta \left[ t \right]}}$$ = $$ - {{\left[ {2.75 - 3} \right]} \over {30}}$$ = $$ + {1 \over {120}}$$ mol L<sup>-1</sup> min<sup>-1</sup>
<br><br>Rate of formation of NO<sub>2</sub> = $$ + {{\Delta \left[ {N{O_2}} ... | mcq | jee-main-2019-online-12th-april-evening-slot | 1,257 |
LzKEZm6Pvx9ZSE16mgjgy2xukf3n9s43 | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | For the reaction<br/> 2A + 3B +
$${3 \over 2}$$C
$$ \to $$ 3P, which
statement is correct ? | [{"identifier": "A", "content": "$${{d{n_A}} \\over {dt}} = {{d{n_B}} \\over {dt}} = {{d{n_C}} \\over {dt}}$$"}, {"identifier": "B", "content": "$${{d{n_A}} \\over {dt}} = {2 \\over 3}{{d{n_B}} \\over {dt}} = {3 \\over 4}{{d{n_C}} \\over {dt}}$$"}, {"identifier": "C", "content": "$${{d{n_A}} \\over {dt}} = {3 \\over 2}... | ["D"] | null | 2A + 3B +
$${3 \over 2}$$C
$$ \to $$ 3P
<br><br>rate = $$ - {1 \over 2}{{d\left[ A \right]} \over {dt}} = - {1 \over 3}{{d\left[ B \right]} \over {dt}} = - {2 \over 3}{{d\left[ C \right]} \over {dt}} = {1 \over 3}{{d\left[ P \right]} \over {dt}}$$
<br><br>$$ \Rightarrow $$ $${{d\left[ A \right]} \over {dt}} = {2 \ove... | mcq | jee-main-2020-online-3rd-september-evening-slot | 1,258 |
nI21ntjnbXvtJjgo6r1kmkjjxk9 | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | The reaction 2A + B<sub>2</sub> $$ \to $$ 2AB is an elementary reaction.<br/><br/>For a certain quantity of reactants, if the volume of the reaction vessel is reduced by a factor of 3, the rate of the reaction increases by a factor of ____________. (Round off to the Nearest Integer). | [] | null | 27 | Let initial concentration of A & B is a & b<br><br>Rate = $$K{[A]^2}{[{B_2}]^1}$$<br><br>$${r_1} = K{\left( {{a \over V}} \right)^2}{\left( {{b \over V}} \right)^1}$$<br><br>$${r_2} = K{\left( {{{3a} \over V}} \right)^2}{\left( {{{3b} \over V}} \right)^1}$$<br><br>$$\left( {{{{r_2}} \over {{r_1}}}} \right) = 27... | integer | jee-main-2021-online-17th-march-evening-shift | 1,259 |
1krxc7you | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | For a chemical reaction A $$\to$$ B, it was found that concentration of B is increased by 0.2 mol L<sup>$$-$$</sup> in 30 min. The average rate of the reaction is ____________ $$\times$$ 10<sup>$$-$$1</sup> mol L<sup>$$-$$1</sup> h<sup>$$-$$1</sup>. (in nearest integer) | [] | null | 4 | A $$\to$$ B<br><br>$$\matrix{
{t = 0} & 0 \cr
{t = 30\,\min } & {0.2M} \cr
} $$<br><br>Av. rate of reaction = $$ - {{\Delta [A]} \over {\Delta t}} = {{\Delta [B]} \over {\Delta t}} = {{(0.2 - 0)} \over {{1 \over 2}}}$$<br><br>$$ = 0.4 = 4 \times {10^{ - 1}}$$ mol / L $$\times$$ hr | integer | jee-main-2021-online-25th-july-evening-shift | 1,260 |
1l5ams8lj | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | <p>For a given chemical reaction</p>
<p>$$\gamma$$<sub>1</sub>A + $$\gamma$$<sub>2</sub>B $$\to$$ $$\gamma$$<sub>3</sub>C + $$\gamma$$<sub>4</sub>D</p>
<p>Concentration of C changes from 10 mmol dm<sup>$$-$$3</sup> to 20 mmol dm<sup>$$-$$3</sup> in 10 seconds. Rate of appearance of D is 1.5 times the rate of disappeara... | [] | null | 1 | Rate $=\frac{1}{r_{1}}\left(\frac{-d[A]}{d t}\right)=\frac{1}{r_{2}}\left(\frac{-d[B]}{d t}\right)=\frac{1}{r_{3}}\left(\frac{-d[C]}{d t}\right)$
<br/><br/>
$$
=\frac{1}{r_{4}}\left(\frac{d[D]}{d t}\right)
$$
<br/><br/>
$\frac{\mathrm{d}[\mathrm{D}]}{\mathrm{dt}}=\frac{\mathrm{r}_{4}}{\mathrm{r}_{2}}\left(\frac{-\mathr... | integer | jee-main-2022-online-25th-june-morning-shift | 1,262 |
1lgv0xz5u | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | <p>$$\mathrm{KClO}_{3}+6 \mathrm{FeSO}_{4}+3 \mathrm{H}_{2} \mathrm{SO}_{4} \rightarrow \mathrm{KCl}+3 \mathrm{Fe}_{2}\left(\mathrm{SO}_{4}\right)_{3}+3 \mathrm{H}_{2} \mathrm{O}$$</p>
<p>The above reaction was studied at $$300 \mathrm{~K}$$ by monitoring the concentration of $$\mathrm{FeSO}_{4}$$ in which initial conc... | [] | null | 333 | The Rate of Reaction (ROR) for a reaction can be calculated based on the changes in concentrations of the reactants or the products over time. In the given reaction,
<br/><br/>$$\mathrm{KClO}_{3}+6 \mathrm{FeSO}_{4}+3 \mathrm{H}_{2} \mathrm{SO}_{4} \rightarrow \mathrm{KCl}+3 \mathrm{Fe}_{2}\left(\mathrm{SO}_{4}\right)... | integer | jee-main-2023-online-11th-april-morning-shift | 1,263 |
1lsg8mpo4 | chemistry | chemical-kinetics-and-nuclear-chemistry | rate-of-reaction | <p>$$\mathrm{NO}_2$$ required for a reaction is produced by decomposition of $$\mathrm{N}_2 \mathrm{O}_5$$ in $$\mathrm{CCl}_4$$ as by equation</p>
<p>$$2 \mathrm{~N}_2 \mathrm{O}_{5(\mathrm{~g})} \rightarrow 4 \mathrm{NO}_{2(\mathrm{~g})}+\mathrm{O}_{2(\mathrm{~g})}$$</p>
<p>The initial concentration of $$\mathrm{N}_2... | [] | null | 17 | <p>Rate of reaction (ROR)</p>
<p>$$\begin{aligned}
& =-\frac{1}{2} \frac{\Delta\left[\mathrm{N}_2 \mathrm{O}_5\right]}{\Delta \mathrm{t}}=\frac{1}{4} \frac{\left[\mathrm{NO}_2\right]}{\Delta \mathrm{t}}=\frac{\Delta\left[\mathrm{O}_2\right]}{\Delta \mathrm{t}} \\
& \mathrm{ROR}=-\frac{1}{2} \frac{\Delta\left[\mathrm{N}... | integer | jee-main-2024-online-30th-january-evening-shift | 1,264 |
Dp6cPMJ2b4MMhzhEsW7k9k2k5eqxpt3 | chemistry | chemistry-in-everyday-life | chemicals-in-foods | The number of sp<sup>2</sup> hybridised carbons present in "Aspartame" is | [] | null | 9 | Strcuture of Aspartame is:
<br><img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264082/exam_images/yd77d5mzs7sc6ycbzh5w.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2020 (Online) 7th January Evening Slot Chemistry - Chemistry in Everyday Life Que... | integer | jee-main-2020-online-7th-january-evening-slot | 1,266 |
Ee1fTQlxcMglJQiUDL1kmkiydfq | chemistry | chemistry-in-everyday-life | chemicals-in-foods | Match List - I with List - II.<br/><br/><table>
<thead>
<tr>
<th></th>
<th>List - I<br/>Chemical Compound</th>
<th></th>
<th>List - II<br/>Used as</th>
</tr>
</thead>
<tbody>
<tr>
<td>(a)</td>
<td>Sucralose</td>
<td>(i)</td>
<td>Synthetic detergent</td>
</tr>
<tr>
<td>(b)</td>
<td>Glyceryl ester of stearic acid</td>
<t... | [{"identifier": "A", "content": "(a)-(i), (b)-(ii), (c)-(iv), (d)-(iii)"}, {"identifier": "B", "content": "(a)-(iii), (b)-(ii), (c)-(iv), (d)-(i)"}, {"identifier": "C", "content": "(a)-(iv), (b)-(iii), (c)-(ii), (d)-(i)"}, {"identifier": "D", "content": "(a)-(ii), (b)-(i), (c)-(iv), (d)-(iii)"}] | ["D"] | null | (a) Sucralose $$ \to $$ Artificial sweetener<br><br>
(b) Glyceryl ester of stearic acid $$ \to $$ Synthetic detergent<br><br>
(c) Sodium benzoate $$ \to $$ Food preservative<br><br>
(d) Bithionol $$ \to $$ Antiseptic | mcq | jee-main-2021-online-17th-march-evening-shift | 1,268 |
1l56azl51 | chemistry | chemistry-in-everyday-life | chemicals-in-foods | <p>Which amongst the following is not a pesticide?</p> | [{"identifier": "A", "content": "DDT"}, {"identifier": "B", "content": "Organophosphates"}, {"identifier": "C", "content": "Dieldrin"}, {"identifier": "D", "content": "Sodium arsenite"}] | ["D"] | null | NaAsO<sub>2</sub> (Sodium arsenite) is an insecticide, antibacterial agent herbicide. | mcq | jee-main-2022-online-28th-june-morning-shift | 1,269 |
1l59qouhu | chemistry | chemistry-in-everyday-life | chemicals-in-foods | <p>Match List I with List II</p>
<p><style type="text/css">
.tg {border-collapse:collapse;border-spacing:0;}
.tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px;
overflow:hidden;padding:10px 5px;word-break:normal;}
.tg th{border-color:black;border-style:solid;bo... | [{"identifier": "A", "content": "A-II, B-III, C-I, D-IV"}, {"identifier": "B", "content": "A-II, B-III, C-IV, D-I"}, {"identifier": "C", "content": "A-III, B-II, C-IV, D-I"}, {"identifier": "D", "content": "A-III, B-II, C-I, D-IV"}] | ["B"] | null | Zymase naturally occurs in yeast.<br/><br/>
Diastase is found in malt.<br/><br/>
Urease is found in soyabean<br/><br/>
Pepsin is found in stomach | mcq | jee-main-2022-online-25th-june-evening-shift | 1,270 |
1l5amaph1 | chemistry | chemistry-in-everyday-life | chemicals-in-foods | <p>Which one of the following is an example of artificial sweetner?</p> | [{"identifier": "A", "content": "Bithional"}, {"identifier": "B", "content": "Alitame"}, {"identifier": "C", "content": "Salvarsan"}, {"identifier": "D", "content": "Lactose"}] | ["B"] | null | Alitame is an aspartic acid-containing sweetener.
<br/><br/>$$
\mathrm{C}_{14} \mathrm{H}_{25} \mathrm{O}_4 \mathrm{N}_3 \mathrm{S}-\text { Alitame }
$$
<br/><br/>First generation artificial sweeteners - Saccharin, cyclamate and aspartame
<br/><br/>Second generation artificial sweeteners - Sucralose, alitame and neotam... | mcq | jee-main-2022-online-25th-june-morning-shift | 1,271 |
1ldppif4t | chemistry | chemistry-in-everyday-life | chemicals-in-foods | <p>Which of the following artificial sweeteners has the highest sweetness value in comparison to cane sugar ?</p> | [{"identifier": "A", "content": "Alitame"}, {"identifier": "B", "content": "Sucralose"}, {"identifier": "C", "content": "Saccharin"}, {"identifier": "D", "content": "Aspartame"}] | ["A"] | null | Sweetness value order wrt cane sugar
<br/><br/>Alitame > Sucralose > Saccharin > Aspartame
<br/><br/>Sucralose = 600
<br/><br/>Aspartame = 100
<br/><br/>Saccharin = 550
<br/><br/>Alitame = 2000 | mcq | jee-main-2023-online-31st-january-morning-shift | 1,272 |
1lh02z8a1 | chemistry | chemistry-in-everyday-life | chemicals-in-foods | <p>Match List I with List II:</p>
<p><style type="text/css">
.tg {border-collapse:collapse;border-spacing:0;}
.tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px;
overflow:hidden;padding:10px 5px;word-break:normal;}
.tg th{border-color:black;border-style:solid;b... | [{"identifier": "A", "content": "A-II, B-III, C-IV, D-I"}, {"identifier": "B", "content": "A-II, B-IV, C-I, D-III"}, {"identifier": "C", "content": "A-II, B-IV, C-III, D-I"}, {"identifier": "D", "content": "A-IV, B-III, C-I, D-II"}] | ["B"] | null | A. Saccharin is first popular artificial sweetening agent. It is 550 times as sweet as cane sugar. It is used as intake by diabetic person.<br/><br/>
B. Aspartame is 100 times as sweet as cane sugar. It is used in cold foods and soft drinks because it is unstable at cooking temperature.<br/><br/>
C. Alitame is 2000 tim... | mcq | jee-main-2023-online-8th-april-morning-shift | 1,273 |
1lh27gxfb | chemistry | chemistry-in-everyday-life | chemicals-in-foods | <p>Match List I with List II</p>
<p><style type="text/css">
.tg {border-collapse:collapse;border-spacing:0;}
.tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px;
overflow:hidden;padding:10px 5px;word-break:normal;}
.tg th{border-color:black;border-style:solid;bo... | [{"identifier": "A", "content": "A-III, B-I, C-IV, D-II"}, {"identifier": "B", "content": "A-IV, B-I, C-III, D-II"}, {"identifier": "C", "content": "A-IV, B-II, C-III, D-I"}, {"identifier": "D", "content": " A-III, B-II, C-IV, D-I"}] | ["A"] | null | <p>We can match the vitamins with their deficiency diseases as follows:</p>
<ul>
<li>Vitamin A: Its deficiency causes Xerophthalmia, so A-III.</li><br/>
<li>Thiamine (Vitamin B1): Its deficiency leads to Beri-Beri, so B-I.</li><br/>
<li>Ascorbic acid (Vitamin C): Its deficiency causes Scurvy, so C-IV.</li><br/>
<li>Rib... | mcq | jee-main-2023-online-6th-april-morning-shift | 1,274 |
lvc58edm | chemistry | chemistry-in-everyday-life | chemicals-in-medicines | <p>Match List I with List II</p>
<p><style type="text/css">
.tg {border-collapse:collapse;border-spacing:0;}
.tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px;
overflow:hidden;padding:10px 5px;word-break:normal;}
.tg th{border-color:black;border-style:solid;bo... | [{"identifier": "A", "content": "A-II, B-IV, C-I, D-III\n"}, {"identifier": "B", "content": "A-III, B-I, C-IV, D-II\n"}, {"identifier": "C", "content": "A-III, B-II, C-IV, D-I\n"}, {"identifier": "D", "content": "A-I, B-II, C-III, D-IV"}] | ["B"] | null | <p>The matching for each compound with its respective use is based on their known applications:</p>
<ul>
<li><strong>Iodoform</strong> is a compound known for its application as an <strong>antiseptic</strong>. It has been used historically in medical applications for the treatment of wounds due to its antimicrobial p... | mcq | jee-main-2024-online-6th-april-morning-shift | 1,275 |
lsaofgdj | chemistry | chemistry-in-everyday-life | cleansing-agents | Match List - I with List - II.
<br/><br/>
<style>
table {
border-collapse: collapse;
width: 100%;
}
th, td {
border: 1px solid black;
padding: 8px;
text-align: left;
}
th {
background-color: blue;
color: white;
}
</style>
<table>
<tr>
<th>List I (Compound)</th>
<th>List II (Use)<... | [{"identifier": "A", "content": "(A)-(II), (B)-(III), (C)-(I), (D)-(IV)"}, {"identifier": "B", "content": "(A)-(III), (B)-(I), (C)-(IV), (D)-(II)"}, {"identifier": "C", "content": "(A)-(I), (B)-(II), (C)-(III), (D)-(IV)"}, {"identifier": "D", "content": "(A)-(IV), (B)-(III), (C)-(II), (D)-(I)"}] | ["B"] | null | <p>Each of the compounds listed in List I has distinct uses. Let's match them correctly with the uses mentioned in List II:</p>
<ul>
<li><strong>Carbon tetrachloride (A)</strong> was historically used as a cleaning agent, among other things, but due to its toxicity and role in ozone depletion, it is no longer widely... | mcq | jee-main-2024-online-1st-february-evening-shift | 1,276 |
1wuw1ZJYf4CjXzFL | chemistry | compounds-containing-nitrogen | aliphatic-amines | Which one of the following methods is neither meant for the synthesis nor for
separation of amines? | [{"identifier": "A", "content": "Hinsberg method"}, {"identifier": "B", "content": "Hofmann method "}, {"identifier": "C", "content": "Wurtz reaction"}, {"identifier": "D", "content": "Curtius reaction"}] | ["C"] | null | Wurtz reaction is for the preparation of hydrocarbons from alkyl halide
<br><br>$$RX + 2Na + XR\buildrel \, \over
\longrightarrow R - R + 2NaX$$ | mcq | aieee-2005 | 1,277 |
hke6MPMCXaonrXTi | chemistry | compounds-containing-nitrogen | aliphatic-amines | Which one of the following is the strongest base in aqueous solution? | [{"identifier": "A", "content": "Trimethylamine "}, {"identifier": "B", "content": "Aniline"}, {"identifier": "C", "content": "Dimethylamine"}, {"identifier": "D", "content": "Methylamine"}] | ["C"] | null | <b>NOTE :</b> Aromatic amines are less basic than aliphatic amines. Among aliphatic amines the order of basicity is $${2^ \circ } > {1^ \circ } > {3^ \circ }.$$ The electron density is decreased in $${3^ \circ }$$ amine due to crowing of alkyl group over $$N$$ atom which makes the approach and bonding by a proton... | mcq | aieee-2007 | 1,278 |
tVO4kJBeRqoqe0Tq | chemistry | compounds-containing-nitrogen | aliphatic-amines | An organic compound A upon reacting with $$N{H_3}$$ gives $$B.$$ On heating $$B$$ gives $$C.$$ $$C$$ in presence of $$KOH$$ reacts with $$B{r_2}$$ to given $$C{H_3}C{H_2}N{H_2}2.$$ $$A$$ is : | [{"identifier": "A", "content": "$$C{H_3}COOH$$ "}, {"identifier": "B", "content": "$$C{H_3}C{H_2}C{H_2}COOH$$ "}, {"identifier": "C", "content": "<img class=\"question-image\" src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734266022/exam_images/anyqajicmjb5ys17ncu5.webp\" loading=\"lazy\" alt=\"JEE Main 201... | ["D"] | null | <img class="question-image" src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265044/exam_images/twoh79gar6mqfxaijtya.webp" loading="lazy" alt="JEE Main 2013 (Offline) Chemistry - Compounds Containing Nitrogen Question 189 English Explanation 1">
<br><br>Reaction $$\left( {{\rm I}{\rm I}{\rm I}} \right)$$ is... | mcq | jee-main-2013-offline | 1,279 |
OW5Yew1POHLRleED | chemistry | compounds-containing-nitrogen | aliphatic-amines | Considering the basic strength of amines in aqueous solution, which one has the smallest pK<sub>b</sub> value? | [{"identifier": "A", "content": "(CH<sub>3</sub>)<sub>3</sub>N"}, {"identifier": "B", "content": "C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub>"}, {"identifier": "C", "content": "(CH<sub>3</sub>)<sub>2</sub>NH"}, {"identifier": "D", "content": "CH<sub>3</sub>NH<sub>2</sub>"}] | ["C"] | null | Arylamines are less basic than alkyl amines and even ammonia. This is due to resonance. In aryl amines the lone pair of electrons on $$N$$ is partly shared with the ring and is thus less available for sharing with a portion.
<br><br>In alkylamines, the electron releasing alkyl group increases the electron density on ni... | mcq | jee-main-2014-offline | 1,280 |
wHLdpNBwztknpOVP | chemistry | compounds-containing-nitrogen | aliphatic-amines | On heating an aliphatic primary amine with chloroform and ethanolic potassium hydroxide, the organic
compound formed is: | [{"identifier": "A", "content": "an alkyl cyanide"}, {"identifier": "B", "content": "an alkyl isocyanide"}, {"identifier": "C", "content": "an alkanol"}, {"identifier": "D", "content": "an alkanediol"}] | ["B"] | null | <img class="question-image" src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265886/exam_images/jfqwx3hqxbnonmgtcqoc.webp" loading="lazy" alt="JEE Main 2014 (Offline) Chemistry - Compounds Containing Nitrogen Question 195 English Explanation"> | mcq | jee-main-2014-offline | 1,281 |
2GYzQ9iPnqF8sJJmBAeQ4 | chemistry | compounds-containing-nitrogen | aliphatic-amines | The test to distinguish primary, secondary and tertiary amines is : | [{"identifier": "A", "content": "Carbylamine reaction"}, {"identifier": "B", "content": "C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl"}, {"identifier": "C", "content": "Sandmeyer\u2019s reaction"}, {"identifier": "D", "content": "Mustard oil test"}] | ["B"] | null | Hinsberg’s reagent (C<sub>6</sub>H<sub>5</sub>SO<sub>2</sub>Cl) forms monoalkyl
sulphonamide with 1<sup>o</sup> amines which is soluble in KOH. With 2<sup>o</sup>
amines it gives dialkyl sulphonamide which is insoluble in KOH
and with 3<sup>o</sup> amines there is no reaction.
<br><br>In mustard oil test, 1<sup>o</sup>... | mcq | jee-main-2016-online-9th-april-morning-slot | 1,283 |
B9RemIihTHRDJ7fS | chemistry | compounds-containing-nitrogen | aliphatic-amines | The increasing order of basicity of the following compounds is :
<img src="data:image/png;base64,UklGRuwQAABXRUJQVlA4IOAQAADwVQCdASoAA5MAPm02l0kkIqIhIZQ5OIANiWlu/HyZFmHnZ12fqb/Qu1v+u/i755/ifzn9w/Kb1YcofWzqffHftP9v/uX7sf3H0jPBH4k/2nqC/lX82/sv5U+hLtBwAfjn9C/y39X/Kb0HP7r0b8QD+Z/2n/dfbX8w97DQG/nH90/3/+E91j+X/7H+U/0H7q+1P8+... | [{"identifier": "A", "content": "(d) < (b) < (a) < (c)"}, {"identifier": "B", "content": "(a) < (b) < (c) < (d)"}, {"identifier": "C", "content": "(b) < (a) < (c) < (d)"}, {"identifier": "D", "content": "(b) < (a) < (d) < (c)"}] | ["D"] | null | Among all the given compounds the basic nature depends upon their tendency to donate the electron pair.
<br><br><img class="question-image" src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734266193/exam_images/y9jvkwbnd0uytf46qgy6.webp" loading="lazy" alt="JEE Main 2018 (Offline) Chemistry - Compounds Contai... | mcq | jee-main-2018-offline | 1,284 |
0J0vkUnXDQ1YBEPrGSAkD | chemistry | compounds-containing-nitrogen | aliphatic-amines | Products A and B formed in the following reactions are respectively :
<br/><br/><img src="data:image/png;base64,UklGRpgMAABXRUJQVlA4IIwMAADQrwCdASoAA6IBP4HA2mW2MC0nIlK40sAwCWlu4WsBG/Pz8+/rVj8uH+n7ny7TZlMPhulf/306ffYa9tgt25y7K7EpqgJKk4Qlpd0Kk6IdfgFViBOGujgeULuhpnw0tLuhpnw0n1bzOVJMaDi6Owwkj4gGX7bxnwTFDJtXBxW7s2CssBY8n39... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1l8g4ppek/de5707f7-766d-4269-a6b6-f380957e27b3/52bfd1c0-3c26-11ed-8acd-3bfc6080b9d7/file-1l8g4ppel.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1l8g4ppek/de5707f7-766d-4269-a6b6-f380957e27b3/52b... | ["D"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l8g4qhru/d640d35f-c40b-46aa-9fab-47c218b3b74a/68a9dda0-3c26-11ed-8acd-3bfc6080b9d7/file-1l8g4qhrv.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l8g4qhru/d640d35f-c40b-46aa-9fab-47c218b3b74a/68a9dda0-3c26-11ed-8acd-3bfc6080b9d7/fi... | mcq | jee-main-2018-online-16th-april-morning-slot | 1,285 |
x8stLU7BwRPYMTAYiV3rsa0w2w9jwva8h07 | chemistry | compounds-containing-nitrogen | aliphatic-amines | The major product of the following reaction is :
<picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267248/exam_images/eulnakid9ch4nait2djf.webp"/><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265733/exam_images... | [{"identifier": "A", "content": "<picture><source media=\"(max-width: 320px)\" srcset=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734264540/exam_images/gajby9zb4d65gja823nu.webp\"><img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734266515/exam_images/cayyykc76stgx8rmnwg2.webp\" style=\"max-width... | ["B"] | null | <picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267369/exam_images/xg0jkpbpsxkgvcq4y0n1.webp"><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264837/exam_images/yodxhw0fvftrrkzzobod.webp"><source media="(max-wid... | mcq | jee-main-2019-online-10th-april-morning-slot | 1,286 |
59BJhaBiyFUZMKkVX83rsa0w2w9jx0tyhjc | chemistry | compounds-containing-nitrogen | aliphatic-amines | Which of the following is not a correct method of the preparation of benzylamine from cyanobenzene ? | [{"identifier": "A", "content": "(i) SnCl<sub>2</sub> + HCl(gas) (ii) NaBH<sub>4</sub>"}, {"identifier": "B", "content": "H<sub>2</sub>/Ni\n"}, {"identifier": "C", "content": "(i) LiAlH<sub>4</sub> &n... | ["D"] | null | <picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267647/exam_images/m1ja8xye3bmxrfrns4vx.webp"><img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264604/exam_images/rjzknonor7hxy5wpsteq.webp" style="max-width: 100%;height: auto;display: block;margi... | mcq | jee-main-2019-online-10th-april-evening-slot | 1,287 |
BmfR8TNQ4WXroQOVbo3rsa0w2w9jwuoung4 | chemistry | compounds-containing-nitrogen | aliphatic-amines | Ethylamine (C<sub>2</sub>H<sub>5</sub>NH<sub>2</sub>) can be obtained from N-ethylphatalimide on treatment with : | [{"identifier": "A", "content": "CaH<sub>2</sub>"}, {"identifier": "B", "content": "H<sub>2</sub>O"}, {"identifier": "C", "content": "NaBH<sub>4</sub>"}, {"identifier": "D", "content": "NH<sub>2</sub>NH<sub>2</sub>"}] | ["D"] | null | N-ethyl phthalimide on treatment with
NH<sub>2</sub>—NH<sub>2</sub> gives ethylamine.
<br><br>It is the final step of Galbriel phatalimide synthesis reaction. | mcq | jee-main-2019-online-10th-april-morning-slot | 1,288 |
P56KeZgF4iXyWbgL0g94w | chemistry | compounds-containing-nitrogen | aliphatic-amines | Which of the following amines can be prepared by Gabriel phthalimide reaction ? | [{"identifier": "A", "content": "neo-pentylamine"}, {"identifier": "B", "content": "n-butylamine"}, {"identifier": "C", "content": "t-butylamine"}, {"identifier": "D", "content": "triethylamine"}] | ["B"] | null | Gabriel phthalimide synthesis is used to prepare 1<sup>o</sup> aliphatic amine.
<picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265031/exam_images/gna0ufltmgbnnvencvui.webp"><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/u... | mcq | jee-main-2019-online-8th-april-morning-slot | 1,290 |
rRfLD2FDqqZzzzktRYfds | chemistry | compounds-containing-nitrogen | aliphatic-amines | A compound 'X' on treatment with Br<sub>2</sub>/NaOH, provided C<sub>3</sub>H<sub>9</sub>N, which gives positive carbylamine test. Compound 'X' is : | [{"identifier": "A", "content": "CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>CONH<sub>2</sub>"}, {"identifier": "B", "content": "CH<sub>3</sub>CON(CH<sub>3</sub>)<sub>2</sub>"}, {"identifier": "C", "content": "CH<sub>3</sub>CH<sub>2</sub>COCH<sub>2</sub>NH"}, {"identifier": "D", "content": "CH<sub>3</sub>COCH<sub>2</sub>... | ["A"] | null | Br<sub>2</sub>/NaOH(Hoffman Hypobromide reagent) converts amide into primary amine having one carbon atom less, which gives
carbylamine test. In the Amide there should be<br> -CONH<sub>2</sub> group to produce primary amine. | mcq | jee-main-2019-online-11th-january-evening-slot | 1,291 |
joRhdIH2URIaz1zoFYDP4 | chemistry | compounds-containing-nitrogen | aliphatic-amines | The major product of the following reaction is :
<br/><br/><img src="data:image/png;base64,UklGRuIIAABXRUJQVlA4INYIAADQXwCdASoAA9cAP4G+1mW2LyqnIdPJOsAwCWlu/HyYv70HZ1+/rr/kP513kf73JI9Qbh7svOV/JGag9B/9ecz9+DqQTG2HtM9pntM9pntM9pntM9pntM9pdc1rHMBwxWscwHDFaxzAZp5KV639zQOGK1jmA4YrXPOr6wHDFaxzAcMVrHMBwa7rOZKKZcwMeqSsO6MVrHMBw... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734266984/exam_images/ptbb3tyal25uotun1g3s.webp\" style=\"max-width: 100%; height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2019 (Online) 10th January Evening Slot Chemistry - Compounds Containi... | ["D"] | null | <picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264067/exam_images/tma1xspoq1yk0hzqukub.webp"><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267503/exam_images/b2hgw3txpybidsfjltv6.webp"><source media="(max-wid... | mcq | jee-main-2019-online-10th-january-evening-slot | 1,292 |
ktLAZ0aAVPn3IiHXaaZGZ | chemistry | compounds-containing-nitrogen | aliphatic-amines | The major product of following reaction is :
<br/><br/><img src="data:image/png;base64,UklGRiARAABXRUJQVlA4IBQRAAAwZwCdASoAA5YAPm02mEekIyKhJFOKaIANiWlu4XKRG/OB8m/37tg/1XSNe+vcXlPROPk/3a/ef3/21fzf+38L+AF7S/1G87gA/Sf675sPynmN4gHBo0A/6J/mvQw/9fNJ9eewv5cPr1IvoP9xI22kEZ0WxI22kEZ0WxI22kEZ0WxI22kEZ0WxI22kEZ0WfenVmWSXhm0ZfTKT... | [{"identifier": "A", "content": "RCOOH"}, {"identifier": "B", "content": "RCONH<sub>2</sub>"}, {"identifier": "C", "content": "RCHO"}, {"identifier": "D", "content": "RCH<sub>2</sub>NH<sub>2</sub>"}] | ["C"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l8mhdmb6/09360d37-5362-4e68-b866-267239bbf4c7/8d39b830-3fa4-11ed-835d-8b6c97a43374/file-1l8mhdmb7.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l8mhdmb6/09360d37-5362-4e68-b866-267239bbf4c7/8d39b830-3fa4-11ed-835d-8b6c97a43374/fi... | mcq | jee-main-2019-online-9th-january-morning-slot | 1,294 |
Nugxl6XAShu0qe9LoYV1Q | chemistry | compounds-containing-nitrogen | aliphatic-amines | The increasing order of the reactivity of the following with LiAlH<sub>4</sub> is
<br/><br/><img src="data:image/png;base64,UklGRmISAABXRUJQVlA4IFYSAACQswCdASoAA4IBP4G+2GW2L6snIbCZWsAwCWlu/EsY3L0HZ1+fqv/h/UF5F2Bhgjmzsv4CLtu0IwK8Kv5zXMTzPhrKeopVMbailUxtqKVTG2opVMbailUxtp6LYu6kq/74W69lwwN4Dhic1s2Z3WPDIx5rpv2jzhs5fe8bwHD... | [{"identifier": "A", "content": "A < B < C < D "}, {"identifier": "B", "content": "B < A < C < D "}, {"identifier": "C", "content": "B < A < D < C "}, {"identifier": "D", "content": "A < B < D < C \n"}] | ["D"] | null | <p>All the given compounds are acid derivatives, thus contain carbonyl group in them. LiAlH<sub>4</sub> reduces these compounds through nucleophilic substitution via addition elimination (S<sub>N<sub>A</sub></sub>E) reaction. The rate of reaction depends upon the following factors:</p>
<p>(i) Size of alkyl group.</p>
<... | mcq | jee-main-2019-online-12th-january-evening-slot | 1,295 |
qT8JE1Nolujt9MAq4O7k9k2k5h2jv28 | chemistry | compounds-containing-nitrogen | aliphatic-amines | The major products A and B in the following reactions are :
<br/><br/><img src="data:image/png;base64,UklGRpYLAABXRUJQVlA4IIoLAABwQwCdASpTAYMAPm02l0gkIyehI3GKiPANiWlu/Gf4wMADOzrs/RX+Pdp39i/JzrZPLH6D+z3pzf0XRN/AHdre//yb+xf7f42fmf+V/jn7Tegvu81AvVH9r/lv7U+dP/PfwD+n98dTL/hfzb2AvZ75N/ff4f/Y/+B/gPQr/jf47/QP917lfU7+9+4B+pf+//... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734267764/exam_images/y2da3abjfzutapcb6kmn.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2020 (Online) 8th January Morning Slot Chemistry - Compounds Containing ... | ["C"] | null | Peroxide generates a radical that abstracts
H-atom from the C-atom adjacent to CN group
to give more stable radical.
<br><br><img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734266940/exam_images/hbntgs4vgfjhad0qhkio.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" a... | mcq | jee-main-2020-online-8th-january-morning-slot | 1,296 |
rkxCXZW1PjLQ7qUzSJjgy2xukfjah2zh | chemistry | compounds-containing-nitrogen | aliphatic-amines | The most appropriate reagent for conversion of
C<sub>2</sub>H<sub>5</sub>CN into CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>NH<sub>2</sub> is | [{"identifier": "A", "content": "NaBH<sub>4</sub>"}, {"identifier": "B", "content": "CaH<sub>2</sub>"}, {"identifier": "C", "content": "Na(CN)BH<sub>3</sub>"}, {"identifier": "D", "content": "LiAlH<sub>4</sub>"}] | ["D"] | null | CH<sub>3</sub>–CH<sub>2</sub>–C$$ \equiv $$N $$\buildrel {LiAl{H_4}} \over
\longrightarrow $$ CH<sub>3</sub>–CH<sub>2</sub>–CH<sub>2</sub>–NH<sub>2</sub> | mcq | jee-main-2020-online-5th-september-morning-slot | 1,297 |
z23SrcXjtoeb27s5vQjgy2xukft5g2f3 | chemistry | compounds-containing-nitrogen | aliphatic-amines | The increasing order of pK<sub>b</sub> values of the
following compounds is :
<br/><br/><img src="data:image/png;base64,UklGRrYYAABXRUJQVlA4IKoYAACQfwCdASr0AeMAPm0ylkikIqIhJHH6IIANiWlu/C1AC+p8ieXqg9TdBM+Gv5J+Nvuu76fsv9m/sn+G/Hn3F/E/oP75/Wv2i/u/sw/E/8e66b5a/lHsx89/wv8Z/qP/O/s3zt/NP8//Kf65/p/7N6U+9T+k/nH7T/AR6e/tv8e/q3+S... | [{"identifier": "A", "content": "I < II < IV < III"}, {"identifier": "B", "content": "I < II < III < IV"}, {"identifier": "C", "content": "II < I < III < IV"}, {"identifier": "D", "content": "II < IV < III < I"}] | ["A"] | null | Order of pK<sub>b</sub>
<img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264860/exam_images/z3mmyt0o1eafgfkf6cez.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2020 (Online) 6th September Morning Slot Chemistry - Compounds Containing Nitrogen Quest... | mcq | jee-main-2020-online-6th-september-morning-slot | 1,298 |
Yu1A602TF5La6xsWfD1kludssqn | chemistry | compounds-containing-nitrogen | aliphatic-amines | An amine on reaction with benzensulphonyl chloride produces a compound insoluble in alkaline solution. This amine can be prepared by ammonolysis of ethyl chloride. The correct structure of amine is : | [{"identifier": "A", "content": "CH<sub>3</sub>CH<sub>2</sub>NH<sub>2</sub>"}, {"identifier": "B", "content": "CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>NHCH<sub>3</sub>"}, {"identifier": "C", "content": "CH<sub>3</sub>CH<sub>2</sub>CH<sub>2</sub>$$\\mathop N\\limits^H $$-CH<sub>2</sub>CH<sub>3</sub>"}, {"identifier": ... | ["C"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734263507/exam_images/jdsgbymcp47dv4yxks2s.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2021 (Online) 26th February Morning Shift Chemistry - Compounds Containing Nitrogen Question 132 English Explana... | mcq | jee-main-2021-online-26th-february-morning-slot | 1,299 |
fVsnuiPkKHTkWjuYUc1kmitlhyd | chemistry | compounds-containing-nitrogen | aliphatic-amines | Which of the following is least basic? | [{"identifier": "A", "content": "$${(C{H_3}CO)_2}\\mathop N\\limits^{..} H$$"}, {"identifier": "B", "content": "$$(C{H_3}CO)\\mathop N\\limits^{..} H{C_2}{H_5}$$"}, {"identifier": "C", "content": "$${({C_2}{H_5})_3}\\mathop N\\limits^{..} $$"}, {"identifier": "D", "content": "$${({C_2}{H_5})_2}\\mathop N\\limits^{..} H... | ["A"] | null | Basic strength $$ \propto $$ availability of lone pair.<br><br>
<img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264786/exam_images/hk5dmevxlchpgshrmsg8.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2021 (Online) 16th March Evening Shift Chemistry... | mcq | jee-main-2021-online-16th-march-evening-shift | 1,301 |
lXqqqlAxX4ZbbG6NXt1kmkisrv9 | chemistry | compounds-containing-nitrogen | aliphatic-amines | Primary, secondary and tertiary amines can be separated using: | [{"identifier": "A", "content": "Chloroform and KOH"}, {"identifier": "B", "content": "Acetyl amide"}, {"identifier": "C", "content": "Benzene sulphonic acid"}, {"identifier": "D", "content": "para-Toluene sulphonyl chloride"}] | ["D"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267245/exam_images/t0biswsxs2am2ueqcyjb.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2021 (Online) 17th March Evening Shift Chemistry - Compounds Containing Nitrogen Question 124 English Explanatio... | mcq | jee-main-2021-online-17th-march-evening-shift | 1,303 |
UwBxxnTsfLvQVeZKog1kmm1esnl | chemistry | compounds-containing-nitrogen | aliphatic-amines | An organic compound "A" on treatment with benzene sulphonyl chloride gives compound B. B is soluble in dil. NaOH solution. Compound A is : | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734265594/exam_images/pwslixewll8snvlbjsfn.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2021 (Online) 18th March Evening Shift Chemistry - Compounds Containing ... | ["A"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734263372/exam_images/wnetimrkxvm3ohyrwchv.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2021 (Online) 18th March Evening Shift Chemistry - Compounds Containing Nitrogen Question 121 English Explanatio... | mcq | jee-main-2021-online-18th-march-evening-shift | 1,305 |
1krq637r5 | chemistry | compounds-containing-nitrogen | aliphatic-amines | Compound A is converted to B on reaction with CHCl<sub>3</sub> and KOH. The compound B is toxic and can be decomposed by C. A, B and C respectively are : | [{"identifier": "A", "content": "primary amine, nitrile compound, conc. HCl"}, {"identifier": "B", "content": "secondary amine, isonitrile compound, conc. NaOH"}, {"identifier": "C", "content": "primary amine, isonitrile compound, conc. HCl"}, {"identifier": "D", "content": "secondary amine, nitrile compound, conc. NaO... | ["C"] | null | <p> Primary amine reacts in presence of chloroform gives isonitrile which is toxic in nature which further reacts in presence of HCl/H<sub>3</sub>O<sup>+</sup> to give primary amine and acid.</p>
<p><img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l2pjg0y6/53c9b964-73e1-4bf1-b1e1-e7d266d7b6de/b0159ee0-c... | mcq | jee-main-2021-online-20th-july-morning-shift | 1,306 |
1krq6tmqs | chemistry | compounds-containing-nitrogen | aliphatic-amines | The number of nitrogen atoms in a semicarbazone molecule of acetone is ______________. | [] | null | 3 | <p>Three nitrogen atoms are present as per structure below</p>
<img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l2pinglb/d5658e35-4c6b-4d1e-a0c6-aac9d986e7aa/95b3cde0-ca86-11ec-ab2b-7960e659c3b6/file-1l2pinglc.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l2pinglb/d5658e35-4c6b... | integer | jee-main-2021-online-20th-july-morning-shift | 1,307 |
1krusgxp0 | chemistry | compounds-containing-nitrogen | aliphatic-amines | Which one of the products of the following reactions does not react with Hinsberg reagent to form sulphonamide? | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734263771/exam_images/a2f10wxv8j6xhfnxj0vd.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2021 (Online) 25th July Morning Shift Chemistry - Compounds Containing N... | ["B"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734266556/exam_images/wmqyxuwqi4mt67fgrosv.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2021 (Online) 25th July Morning Shift Chemistry - Compounds Containing Nitrogen Question 112 English Explanation... | mcq | jee-main-2021-online-25th-july-morning-shift | 1,308 |
1ks1iikga | chemistry | compounds-containing-nitrogen | aliphatic-amines | What is A in the following reaction?<br/><br/><picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734266984/exam_images/d0emlfqryfw73ldvvucm.webp"/><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265791/exam_images/bw9... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734265762/exam_images/zwjgezkf8rc23mncnhc1.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2021 (Online) 27th July Evening Shift Chemistry - Compounds Containing N... | ["D"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734266430/exam_images/ififp5coojbveagaiqed.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2021 (Online) 27th July Evening Shift Chemistry - Compounds Containing Nitrogen Question 105 English Explanation... | mcq | jee-main-2021-online-27th-july-evening-shift | 1,310 |
1ktcre441 | chemistry | compounds-containing-nitrogen | aliphatic-amines | <picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264790/exam_images/zhzneufk6dzfbruyccij.webp"/><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265472/exam_images/noupzorfncrbyfcf5wyk.webp"/><source media="(max-w... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734266648/exam_images/g4pxejyphxmhrzbqhi16.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2021 (Online) 26th August Evening Shift Chemistry - Compounds Containing... | ["C"] | null | <p>Cyanohydrin is formed when carbonyl compound reacts with HCN in the presence of alkali (NaOH).</p>
<img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l3xamdbr/05deeb0a-3875-43a4-9bfb-60efebd159e5/aae99070-e299-11ec-8ea3-fd6d660fc854/file-1l3xamdbs.png?format=png" data-orsrc="https://app-content.cdn.exa... | mcq | jee-main-2021-online-26th-august-evening-shift | 1,311 |
1ktebsbu3 | chemistry | compounds-containing-nitrogen | aliphatic-amines | The major product of the following reaction is :<br/><br/><picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267028/exam_images/hri77qeonxxrpaaxjkxn.webp"/><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264366/exa... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734264959/exam_images/vbvu8ebcxl3epzxdchco.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2021 (Online) 27th August Morning Shift Chemistry - Compounds Containing... | ["C"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265375/exam_images/jyjisl6t1yfwzw5cwc6c.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2021 (Online) 27th August Morning Shift Chemistry - Compounds Containing Nitrogen Question 98 English Explanatio... | mcq | jee-main-2021-online-27th-august-morning-shift | 1,312 |
1ktebukq3 | chemistry | compounds-containing-nitrogen | aliphatic-amines | Which of the following is not a correct statement for primary aliphatic amines? | [{"identifier": "A", "content": "The intermolecular association in primary amines is less than the intermolecular association in secondary amines."}, {"identifier": "B", "content": "Primary amines on treating with nitrous acid solution from corresponding alcohols except mythyl amine."}, {"identifier": "C", "content": "... | ["A"] | null | The intermolecular association is more prominent in case of primary amines as compared to secondary, due to the availability of two hydrogen atom. | mcq | jee-main-2021-online-27th-august-morning-shift | 1,313 |
1ktiabu87 | chemistry | compounds-containing-nitrogen | aliphatic-amines | The major products A and B in the following set of reactions are :<br/><br/><img src="data:image/png;base64,UklGRpwNAABXRUJQVlA4IJANAADQTACdASrOAWcAPm0ylkgkIqIhJhG6YIANiWlu/HyXu8ANf0DwnafGX8c/HfzH/qP9m/rn7M+JL51+8/lP/YfXC+GOor/ov5X3Unvv8f/r/+69Sf8t/Qv6H/rv6r6K/BzUL9Kf3D+R/t9/Y/T1/ev4B3lFbP0W9gj3d+b/5L+gfz3/t/3Lzwv4L+fe... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734267242/exam_images/fvx7vreu5jxr9gls6hs4.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2021 (Online) 31st August Morning Shift Chemistry - Compounds Containing... | ["B"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734266125/exam_images/vntvp8qezycm0smopmqs.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2021 (Online) 31st August Morning Shift Chemistry - Compounds Containing Nitrogen Question 95 English Explanatio... | mcq | jee-main-2021-online-31st-august-morning-shift | 1,314 |
1l57selme | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>Given below are two statements :</p>
<p>Statement I : In Hofmann degradation reaction, the migration of only an alkyl group takes place from carbonyl carbon of the amide to the nitrogen atom.</p>
<p>Statement II : The group is migrated in Hofmann degradation reaction to electron deficient atom.</p>
<p>In the light o... | [{"identifier": "A", "content": "Both Statement I and Statement II are correct."}, {"identifier": "B", "content": "Both Statement I and Statement II are incorrect."}, {"identifier": "C", "content": "Statement I is correct but Statement II is incorrect."}, {"identifier": "D", "content": "Statement I is incorrect but Sta... | ["D"] | null | Hofmann bromamide degradation
<br/><br/>
In this degradation, the migration of the alkyl/aryl group occurs to the electron-deficient nitrogen (nitrene).
<br/><br/>
Statement (I) is not absolutely correct as it mentions only the alkyl group, whereas migration of aryl groups may also occur depending on migratory aptitude... | mcq | jee-main-2022-online-27th-june-morning-shift | 1,315 |
1l59rcbl1 | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>Which of the following ketone will NOT give enamine on treatment with secondary amines? [where t-Bu is $$-$$C(CH<sub>3</sub>)<sub>3</sub>]</p> | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1l5bre8zv/ea93985e-300c-4136-9e2d-fd8271bb5141/74c2adb0-fe5a-11ec-b169-b5046c590266/file-1l5bre8zw.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1l5bre8zv/ea93985e-300c-4136-9e2d-fd8271bb5141/74c... | ["C"] | null | In order to form enamine from the reaction of carbonyl compound with $2^{\circ}$ amine, the carbonyl compound must have $\alpha$-hydrogen.<br><br><img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l9xoluds/99e3480f-fb77-4671-9d19-388cb23f9f65/a85c4100-5999-11ed-8313-678a7ff0eccc/file-1l9xoludt.png?format=... | mcq | jee-main-2022-online-25th-june-evening-shift | 1,318 |
1l5am871r | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>The reaction of <img src="data:image/png;base64,UklGRr4HAABXRUJQVlA4ILIHAABQlQCdASoAA6ABP4HA32S2Mj+nIdTZK/AwCWlu4WuUDmNwvVSIfdKcs6Mg0O5Cf7gvcF7gvcF7gvcF7gvcF7gvcF7gvb+4opePcUUvHuKKXj3FFLx7iil49xRS8e4op1hS8e4opePcUUvHuKKXj3FFLx7iil49xRS8lRhACzJ58jKzMfztgil49xP0kmxtG0buGIwUmyNqJ9UDzm/K26tGuzhVQdNUCxuo/rhvgUVlByjuun6Q5... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1l5bsrsgh/60f1004d-c79d-4975-b4c4-c1a9d526c905/d6712410-fe5f-11ec-b169-b5046c590266/file-1l5bsrsgi.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1l5bsrsgh/60f1004d-c79d-4975-b4c4-c1a9d526c905/d67... | ["C"] | null | The given reaction is Hoffmann-Bromide degradation method.<br><br><img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l8mcz7ju/2b08e754-fa9e-405e-9596-0e7eeabfe921/57fb1ad0-3f93-11ed-af9d-134e99e746ec/file-1l8mcz7jx.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l8mcz7ju/2b08e754-f... | mcq | jee-main-2022-online-25th-june-morning-shift | 1,319 |
1l6e1oe02 | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>An organic compound 'A' on reaction with NH<sub>3</sub> followed by heating gives compound B. Which on further strong heating gives compound C (C<sub>8</sub>H<sub>5</sub>NO<sub>2</sub>). Compound C on sequential reaction with ethanolic KOH, alkyl chloride and hydrolysis with alkali gives a primary amine. The compoun... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1l6er17kp/dc2fdf54-8df8-40b7-9ee0-d2c6d0729fd7/9b788890-13cb-11ed-b12e-0be2f600acf7/file-1l6er17kq.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1l6er17kp/dc2fdf54-8df8-40b7-9ee0-d2c6d0729fd7/9b7... | ["C"] | null | <p>Gabriel Pthalimide reaction</p><p><img src="https://app-content.cdn.examgoal.net/fly/@width/image/1lc5nql4j/e8fc9730-d481-445f-aeb2-f7e56ce4790e/f7144c30-8594-11ed-a4e1-239777dab634/file-1lc5nql4k.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1lc5nql4j/e8fc9730-d481-445f-aeb2-f7e56ce4790e/f7... | mcq | jee-main-2022-online-25th-july-morning-shift | 1,321 |
1l6e2hux2 | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>The number of sp<sup>3</sup> hybridised carbons in an acyclic neutral compound with molecular formula C<sub>4</sub>H<sub>5</sub>N is ___________.</p> | [] | null | 1 | $\mathrm{C}_{4} \mathrm{H}_{5} \mathrm{~N}$
<br><br>
$$
\begin{aligned}
\mathrm{DBE} & =(\mathrm{C}+1)-\left(\frac{\mathrm{H}+\mathrm{X}-\mathrm{N}}{2}\right) \\\\
& =4+1-\left(\frac{5-1}{2}\right)=5-2=3
\end{aligned}
$$
<br><br>
3 double bond equivalent are present in compound<br><br>
<img src="https://app-con... | integer | jee-main-2022-online-25th-july-morning-shift | 1,322 |
1l6jmd7lc | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>Match List I with List II.</p>
<p><style type="text/css">
.tg {border-collapse:collapse;border-spacing:0;}
.tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px;
overflow:hidden;padding:10px 5px;word-break:normal;}
.tg th{border-color:black;border-style:solid;b... | [{"identifier": "A", "content": "A-IV, B-III, C-II, D-I"}, {"identifier": "B", "content": "A-IV, B-II, C-I, D-III"}, {"identifier": "C", "content": "A-III, B-IV, C-I, D-II"}, {"identifier": "D", "content": "A-IV, B-III, C-I, D-II"}] | ["C"] | null | (A) Benzene sulphonyl chloride is also known as Hinsberg reagent.
<br/><br/>
(B) Hoffmann bromamide reaction involves conversion of amide to amine having one $\mathrm{C}$ atom less. This reaction involves isocyanate as intermediate.
<br/><br/>
(C) Carbylamine reaction is a test given by all primary amines.
<br/><br/>
(... | mcq | jee-main-2022-online-27th-july-morning-shift | 1,323 |
1l6mdl525 | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>Identify the correct statement for the below given transformation.</p>
<p><img src="data:image/png;base64,UklGRoYXAABXRUJQVlA4IHoXAAAwdQCdASoAA3UAPm02l0gkIyIhI7JKuIANiWlu/HyZbsADOzrn/UD+vfjb4Mf4z8oPPvxce3/Y/2Cf6rwf9f+Z/8q+0n6L+zfuX/gPnD/Ff4/wx+aH+H6gX5L/M/83+Y/BXgC/O/7F/yf8R4yOpx4R/6PuAfzj+0+nX+y8K77r/0vYG/mP+H9Db/0... | [{"identifier": "A", "content": "$$\\mathrm{A}-\\mathrm{CH}_{3} \\mathrm{CH}_{2} \\mathrm{CH}=\\mathrm{CH}-\\mathrm{CH}_{3}, \\mathrm{~B}-\\mathrm{CH}_{3} \\mathrm{CH}_{2} \\mathrm{CH}_{2} \\mathrm{CH}=\\mathrm{CH}_{2}$$, Saytzeff products"}, {"identifier": "B", "content": "$$\\mathrm{A}-\\mathrm{CH}_{3} \\mathrm{CH}_{... | ["C"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l7ox98ww/972cdfcc-dc88-4d3a-af89-fcaaa1d73196/ffa06d10-2d2f-11ed-b144-5949e1cb6ba8/file-1l7ox98wx.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l7ox98ww/972cdfcc-dc88-4d3a-af89-fcaaa1d73196/ffa06d10-2d2f-11ed-b144-5949e1cb6ba8/fi... | mcq | jee-main-2022-online-28th-july-morning-shift | 1,324 |
1l6p7bpbr | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>Which among the following is the strongest Bronsted base?</p> | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1l6sdqjaq/9ba6d3f6-a138-4780-858d-df2ca7e3d6b5/9509f120-1b4a-11ed-a30a-c150b936f917/file-1l6sdqjar.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1l6sdqjaq/9ba6d3f6-a138-4780-858d-df2ca7e3d6b5/950... | ["D"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l7w079b9/3124b409-015b-4635-a315-51295392cf64/003fd150-3115-11ed-aea7-cb6fb344ee54/file-1l7w079ba.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l7w079b9/3124b409-015b-4635-a315-51295392cf64/003fd150-3115-11ed-aea7-cb6fb344ee54/fi... | mcq | jee-main-2022-online-29th-july-morning-shift | 1,325 |
1l6rkx939 | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>The Hinsberg reagent is</p> | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1l6tc4qar/07d8f542-cb7d-496f-b9db-e506bfb5620c/162a7730-1bd1-11ed-9f1d-eff1e78b91ab/file-1l6tc4qas.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1l6tc4qar/07d8f542-cb7d-496f-b9db-e506bfb5620c/162... | ["A"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l6tc4qar/07d8f542-cb7d-496f-b9db-e506bfb5620c/162a7730-1bd1-11ed-9f1d-eff1e78b91ab/file-1l6tc4qas.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l6tc4qar/07d8f542-cb7d-496f-b9db-e506bfb5620c/162a7730-1bd1-11ed-9f1d-eff1e78b91ab/fi... | mcq | jee-main-2022-online-29th-july-evening-shift | 1,326 |
1ldojf2re | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>In the following reaction, 'A' is</p>
<p><img src="data:image/png;base64,UklGRmAJAABXRUJQVlA4IFQJAADQbACdASoAA+oAP4G21mY2LKwnIfDJSsAwCWlu4WdzlmNwvV6PtL7QDtLl4A5m36JwM4t/oKi2YA7p+yy5jxY/dD2P7cFUCbkadun7f6CotmAO5z6wGJJidwGoVkJYHGtMXs4K0wcRI6vOaWfMbwGmAWpPI8FOLYEWyxMks+Y3gOGBzSz5yjmlm5hxws8XjI2H7qkceXIDpkOAqycKjZjeA4YH... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1ldoupxop/4856410c-1aa8-4465-a7e2-a39d7e1b4faf/60982b90-a3ef-11ed-b56d-63317aef4a22/file-1ldoupxoq.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1ldoupxop/4856410c-1aa8-4465-a7e2-a39d7e1b4faf/609... | ["B"] | null | <p>Initially lone pair electron of –NH<sub>2</sub> attack on
electrophilic carbon, after then lone pair electron of
oxygen attacks leading to formation of cyclic
compound. </p>
<p><img src="https://app-content.cdn.examgoal.net/fly/@width/image/1ldx66aoy/ad3250b5-6ddc-4cae-8d07-93409192ff27/71344820-a882-11ed-99b3-79cb2... | mcq | jee-main-2023-online-1st-february-morning-shift | 1,328 |
1ldscxm1g | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>Reaction of propanamide with $$\mathrm{Br_2/KOH(aq)}$$ produces :</p> | [{"identifier": "A", "content": "Propanenitrile"}, {"identifier": "B", "content": "Propylamine"}, {"identifier": "C", "content": "Ethylnitrile"}, {"identifier": "D", "content": "Ethylamine"}] | ["D"] | null | <p>Propanamide $$\mathrm{\buildrel {B{r_2}/KOH} \over
\longrightarrow}$$ Ethylamine</p> | mcq | jee-main-2023-online-29th-january-evening-shift | 1,329 |
1ldsqid48 | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>The major product 'P' for the following sequence of reactions is :</p>
<p><img src="data:image/png;base64,UklGRpoWAABXRUJQVlA4II4WAADwfQCdASoAA8UAPm02mEikIyKhI3MpgIANiWlu/GwZqMV+3LRkpN+SP7T2v/4v8lfQ/xjehfc3kTRRPjv3C/Uf2n92vjD/M96fxk/u/tk+QX8f/oP+T3tvcP836BHsN9R/4nhd/6noT9gvYA/XT0574v8X6gv9M/xXoVfW3oJ+rv2s+A/+e/4H/vd... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1ldt1hres/fc70c853-8425-4db6-976b-8bdc37a992bc/ffc67c40-a63c-11ed-8e98-03be028140e9/file-1ldt1hret.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1ldt1hres/fc70c853-8425-4db6-976b-8bdc37a992bc/ffc... | ["B"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1lekox0np/25ee036a-96d1-4352-af2d-ed1ab7876f2d/c38f6540-b571-11ed-b96f-23ae160a1d3b/file-1lekox0nq.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1lekox0np/25ee036a-96d1-4352-af2d-ed1ab7876f2d/c38f6540-b571-11ed-b96f-23ae160a1d3b/fi... | mcq | jee-main-2023-online-29th-january-morning-shift | 1,330 |
1ldwuow3h | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>Given below are two statements :</p>
<p><img src="data:image/png;base64,UklGRkYNAABXRUJQVlA4IDoNAACQQwCdASoAA1kAPm02mEikIyKhJBI5qIANiWlu4XVRG/Or8ef1nta/uv5I+f/iq9ofrnmpZa+rL/A9DP5b9p/1H9z8z+8f4OagXrD/WeGXsCrM+gF69fWf+J3/f8p6F/XP+++4B+rv+k8m7wBvHfYA/m39K/5H9w90z+k/ZXzlfnv+M/+H+X+AP+cf2z/xdfX0gf3cHdFlYR8C4TUW6dWacns7p... | [{"identifier": "A", "content": "Both Statement I and Statement II are true"}, {"identifier": "B", "content": "Statement I is false but Statement II is true"}, {"identifier": "C", "content": "Statement I is true but Statement II is false"}, {"identifier": "D", "content": "Both Statement I and Statement II are false"}] | ["C"] | null | <p><img src="https://app-content.cdn.examgoal.net/fly/@width/image/1lenn9nry/e658c015-f37c-4a13-85dd-82be71c3cca8/aad18be0-b711-11ed-9724-4158dd188df0/file-1lenn9nrz.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1lenn9nry/e658c015-f37c-4a13-85dd-82be71c3cca8/aad18be0-b711-11ed-9724-4158dd188df0... | mcq | jee-main-2023-online-24th-january-evening-shift | 1,331 |
1ldyh2v2q | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>Increasing order of stability of the resonance structures is :</p>
<p><img src="data:image/png;base64,UklGRlgXAABXRUJQVlA4IEwXAACQJgGdASoAA6sCP4G82GY2Lr+nIZE5Q/AwCWlu/FpuYZSTgu9M8bfDz3/vcb3w3/M9sPOf2a/mv8H///3/09kAv359RSm5+TfzP//6aPvsOfQzaGbQzaGbQzaGbQzaGbQzaGbQzaFu4jnDFMRzhimI5wxTEc4YpbWLDw4pLiOcMUxHSntV7yhqrgPZd7B... | [{"identifier": "A", "content": "D, C, B, A"}, {"identifier": "B", "content": "C, D, B, A"}, {"identifier": "C", "content": "C, A, B, D "}, {"identifier": "D", "content": "D, C, A, B"}] | ["C"] | null | Correct stabilising order is $$C < A < B < D$$ | mcq | jee-main-2023-online-24th-january-morning-shift | 1,332 |
lgo06mre | chemistry | compounds-containing-nitrogen | aliphatic-amines | Decreasing order of reactivity towards electrophilic substitution for the following compounds is :<br/><br/>
<img src="data:image/png;base64,UklGRsALAABXRUJQVlA4ILQLAACQiwCdASoAAxoBP4HA2mQ2MK0mo3H5osAwCWlu9T+FPG3Rs5lc3mP/U2s/5ntN58u1X5WKEqvPo/SdXn5kZi2LpUOplQyDjTggXtgUiswPa0AHn4wSodTKhkHGnDqZUMUe7cQawj/SUu7cBmfXbP4s1sQ... | [{"identifier": "A", "content": "$ \\mathrm{a}>\\mathrm{d}>\\mathrm{e}>\\mathrm{b}>\\mathrm{c}$"}, {"identifier": "B", "content": "$\\mathrm{d}>\\mathrm{a}>\\mathrm{e}>\\mathrm{c}>$ b"}, {"identifier": "C", "content": "$\\mathrm{c}>\\mathrm{b}>\\mathrm{a}>\\mathrm{d}>\\mathrm{e}$"}, {"identifier": "D", "content": "$\\m... | ["D"] | null | Higher the electron density on Benzene Ring, Higher its Reactivity towards electrophilic substitution Reaction<br><br>
<img src="https://app-content.cdn.examgoal.net/fly/@width/image/1lgrla7sj/dabe1eb5-e9f4-4308-94ba-d1f6c3873dc6/7960b430-e0d5-11ed-ac7f-75b667b9d8cc/file-1lgrla7sk.png?format=png" data-orsrc="https://ap... | mcq | jee-main-2023-online-15th-april-morning-shift | 1,333 |
1lgq4i2lp | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>In the reaction given below</p>
<p><img src="data:image/png;base64,UklGRhobAABXRUJQVlA4IA4bAAAwjgCdASoAA8QAPm02l0gkIyIhJLIp6IANiWlu5VART8Rvzh/GH9m/Hbwf/xv5R+iP439H/nf7V+4/9x5cXXvmr/J/vT+Z/sv+D99n8x3t/LLUF/J/5p/ePtc9RP+77YO2/oC+1v1D/kf3L1ZvqvNH7G+wBwWvpvsB/0f/Rerj/c+Oj6z9g39ff+X69HsC9LUh64usLTpAnH9KzE4R0dKGqN543vbm80... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1lgqz8mft/74dfe0bf-9bf9-4b80-a308-b4a106dd96ed/443b7890-e07f-11ed-baf9-87204e3a7c88/file-1lgqz8mfu.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1lgqz8mft/74dfe0bf-9bf9-4b80-a308-b4a106dd96ed/443... | ["C"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1lh1pt63p/d7289697-e7c7-4a55-908e-4dc1cbb54058/03751c60-e667-11ed-b7c9-957e12d0338a/file-1lh1pt63q.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1lh1pt63p/d7289697-e7c7-4a55-908e-4dc1cbb54058/03751c60-e667-11ed-b7c9-957e12d0338a/fi... | mcq | jee-main-2023-online-13th-april-morning-shift | 1,334 |
1lgvtxa6z | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>In the reaction given below:</p>
<p><img src="data:image/png;base64,UklGRlYIAABXRUJQVlA4IEoIAACwbgCdASoAA/8AP4HA3GQ2Mbumo3S5E3AwCWluy2AJ/aV1eZbS+zq7Y9875t0S7xtT+EPtaOMyU4oUBYBGTtpGmQksbvWN3rG71jd6xu9Y3esbvWNhQcgwCNZiEED1Ka6Id8zu+4DxicjmtXzO77gPGJyOa1fM797izbPslYF57M7vuA8YnI5rV8zu+4DxicjmtXzO7793ONJmv8zvBca1fM7vuA8Yn... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1lgx3jpbk/0646dfa7-754a-4da6-8980-d90be2dff781/d0c5af00-e3dc-11ed-baaf-253646c1f54e/file-1lgx3jpbl.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1lgx3jpbk/0646dfa7-754a-4da6-8980-d90be2dff781/d0c... | ["A"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/6y3zli1lixpydog/e3464748-32e4-4801-8692-49cfaaf9bb73/e083ec00-0bcc-11ee-acbf-7f9d4e788425/file-6y3zli1lixpydoh.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/6y3zli1lixpydog/e3464748-32e4-4801-8692-49cfaaf9bb73/e083ec00-0bcc-11ee-ac... | mcq | jee-main-2023-online-10th-april-evening-shift | 1,335 |
1lh28tqxq | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>The major product formed in the following reaction is</p>
<p><img src="data:image/png;base64,UklGRowJAABXRUJQVlA4IIAJAACwfACdASoAAwMBP4HA2WS2MCynI3HpOsAwCWlu4XHhG/Pn9IfqZbe2cXan5++hQjWq/+nFT/9yH//6qDYNsTgbYnA2xOBticDbE4G2JwNsTgbYmmY2qpQ4mdkVdXKb0oYA52tCB6hJFc3D+a7+dvtbi7UQiEQiEQiEQiERBBg8wmvSr/hTmhBUvLJZBmYr4TXY9+WY... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1lh30to97/7ba3dfbb-74ce-4717-a880-46cd496067df/de8cadb0-e71e-11ed-ab3e-bf3b57063390/file-1lh30to98.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1lh30to97/7ba3dfbb-74ce-4717-a880-46cd496067df/de8... | ["D"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/6y3zli1llmldc59/2160c215-b42c-4484-970a-c47c5b949892/f9d0c6d0-4112-11ee-8398-91a6dbfb2303/file-6y3zli1llmldc5a.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/6y3zli1llmldc59/2160c215-b42c-4484-970a-c47c5b949892/f9d0c6d0-4112-11ee-83... | mcq | jee-main-2023-online-6th-april-morning-shift | 1,336 |
lvb2abdo | chemistry | compounds-containing-nitrogen | aliphatic-amines | <p>An amine $$(\mathrm{X})$$ is prepared by ammonolysis of benzyl chloride. On adding p-toluenesulphonyl chloride to it the solution remains clear. Molar mass of the amine $$(\mathrm{X})$$ formed is _________ $$\mathrm{g} \mathrm{mol}^{-1}$$.</p>
<p>(Given molar mass in $$\mathrm{gmol}^{-1} \mathrm{C}: 12, \mathrm{H}: ... | [] | null | 287 | <p><img src="https://app-content.cdn.examgoal.net/fly/@width/image/1lwbneomw/80cd3ff6-b58f-4bd3-ac16-0f6be1ccb3a3/b38e3b80-14d4-11ef-8218-dfd8f7832166/file-1lwbneomx.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1lwbneomw/80cd3ff6-b58f-4bd3-ac16-0f6be1ccb3a3/b38e3b80-14d4-11ef-8218-dfd8f7832166... | integer | jee-main-2024-online-6th-april-evening-shift | 1,338 |
HHZDJBjTpKAd5kdVSdnUK | chemistry | compounds-containing-nitrogen | aromatic-amines | The major product expected from the following reaction is :
<br/><br/><img src="data:image/png;base64,UklGRigKAABXRUJQVlA4IBwKAACQfACdASoAA/MAP4G82GU2LqynInGposAwCWlu4W5TqmNwu4+Hq+OD/5Tc09q80AHlxWf5f/89PxuJIUhJaCJOXKlIm3tfAA9VTKLrgL1XAlmvJx5kKWgRaq+Ref1VVYB9u+TYWVVgH275MMOAt9fJyx5cU5qFMeO1uSjjXaJ7e2+9YQUDb4hGs3MLnWk7f... | [{"identifier": "A", "content": "<img src=\"https://app-content.cdn.examgoal.net/fly/@width/image/1l83n158e/546a352d-a34b-4ba3-b75f-a23c1199a4c6/c4c26de0-3547-11ed-8c5c-f3f0850e6b94/file-1l83n158f.png?format=png\" data-orsrc=\"https://app-content.cdn.examgoal.net/image/1l83n158e/546a352d-a34b-4ba3-b75f-a23c1199a4c6/c4c... | ["C"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l83n1q7w/6e34ab7e-71e4-4df5-a7e8-88df3a2789d5/d4f883c0-3547-11ed-8c5c-f3f0850e6b94/file-1l83n1q7x.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l83n1q7w/6e34ab7e-71e4-4df5-a7e8-88df3a2789d5/d4f883c0-3547-11ed-8c5c-f3f0850e6b94/fi... | mcq | jee-main-2017-online-8th-april-morning-slot | 1,339 |
PNTwLIvaUKMvYWywfYb4Y | chemistry | compounds-containing-nitrogen | aromatic-amines | Arrange the following amines in the decreasing order of basicity :
<br/><br/><img src="data:image/png;base64,UklGRtYPAABXRUJQVlA4IMoPAADQ9gCdASoAAzoCP4HA3GS2Mb+nIpOJQ/AwCWlu6//AwUn9ljRkpzeqv9160Ol/nr+J4Rv/b5/O435TfeHR1wZFf/RC//9itE56KH//9R/4p//xEl5mEc4UVLiOf1DVS70SAvxFFdDMdMAANcJKLs+oIfUEPqCHyeRaFkdzWSybIe3zp7YVDMMBbe... | [{"identifier": "A", "content": "I > II > III"}, {"identifier": "B", "content": "III > I > II"}, {"identifier": "C", "content": "III > II > I"}, {"identifier": "D", "content": "I > III > II"}] | ["B"] | null | <img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l8mi4zfy/8138752c-9849-480e-a4e2-2c102343462a/863768e0-3fa7-11ed-835d-8b6c97a43374/file-1l8mi4zfz.png?format=png" data-orsrc="https://app-content.cdn.examgoal.net/image/1l8mi4zfy/8138752c-9849-480e-a4e2-2c102343462a/863768e0-3fa7-11ed-835d-8b6c97a43374/fi... | mcq | jee-main-2019-online-9th-january-morning-slot | 1,340 |
JOPBGdz1AkriyAbfNtN9f | chemistry | compounds-containing-nitrogen | aromatic-amines | The major product of the following reaction is:
<img src="data:image/png;base64,UklGRqAUAABXRUJQVlA4IJQUAACwugCdASr1AmABP4G81mU2Lr+nIfGZ0/AwCWlu8pDb/QUZExu9bh8of6b1BfQP4jaFcLbRTsT4BHsv9Xt+LAB+U+aFMp+/ZdLww6AH8K9Jf/y8nn7z/6/389P/tli2wTTD27gmmHt3BNMPbuCaYe3cE0w9u4EVRH+Q7yMMNJ/8dRAh3kYYZN5GGGTeRhhk3lpyLWomBe+lJlSb80+7ZeBn... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734267490/exam_images/vqqczz5mtfl0xxfqnpp8.webp\" style=\"max-width: 100%; height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2019 (Online) 8th April Evening Slot Chemistry - Compounds Containing ... | ["D"] | null | <picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267550/exam_images/yaf0iew5glsqxqvxy0ev.webp"><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267557/exam_images/iaeewpmgjqgvxnuyz7zg.webp"><source media="(max-wid... | mcq | jee-main-2019-online-8th-april-evening-slot | 1,341 |
73PmFf1SvCQa1RSCMot9m | chemistry | compounds-containing-nitrogen | aromatic-amines | The increasing order of reactivity of the following compounds towards reaction with alkyl halides directly is
<img src="data:image/png;base64,UklGRkYPAABXRUJQVlA4IDoPAABQZACdASq0AUUBPm00l0kkIqIhIhIpOIANiWlu/Eb5FoBHZ11fop/Hfx+8GP773Dfm/7t+Sf5I8B18o95h7t/L/63/0f6d86P139G/F/33/C/sBfk/8Z/r/8c/sH9y/Nb24f6r+H/y3wPqsfqB7Avcn... | [{"identifier": "A", "content": "A < B < C < D"}, {"identifier": "B", "content": "B < A < C < D"}, {"identifier": "C", "content": "B < A < D < C"}, {"identifier": "D", "content": "A < C < D < B"}] | ["B"] | null | Lone pair over nitrogen will act as the reacting centre and more free nitrogen atom will be more reactive towards alkyl halide.
<br><br>For compound (A), lone pair of N atom is in resonance with $$\pi $$ bond of C = O. So lone pair of N atom gets delocalised.
<br><br>For compound (B), lone pair of N atom is in resonanc... | mcq | jee-main-2019-online-12th-january-morning-slot | 1,342 |
dy0TwBKtVzcnRZv4Osw7f | chemistry | compounds-containing-nitrogen | aromatic-amines | An aromatic compound 'A' having molecular formula C<sub>7</sub>H<sub>6</sub>O<sub>2</sub> on treating with aqueous ammonia and heating forms compound 'B'. The compound 'B' on reaction with molecular bromine and potassium hydroxide provides compound 'C' having molecular formula C<sub>6</sub>H<sub>7</sub>N.. The structur... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734267150/exam_images/ir1e3cbvtjgh3poenatq.webp\" style=\"max-width: 100%; height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2019 (Online) 10th January Evening Slot Chemistry - Compounds Containi... | ["B"] | null | <picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734266478/exam_images/o1ulr3jzzdtluo332yrm.webp"><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265249/exam_images/pem1rwuerviwa4atfvr2.webp"><source media="(max-wid... | mcq | jee-main-2019-online-10th-january-evening-slot | 1,343 |
NtOU10wGVAjgXloUC67k9k2k5dzwz5z | chemistry | compounds-containing-nitrogen | aromatic-amines | Consider the following reaction :<br/><br/>
<img src="data:image/png;base64,UklGRqYLAABXRUJQVlA4IJoLAAAQSwCdASrKAZcAPm02mEikIyKhI5KJyIANiWlu4XJ+KxnZ13/o7/W+1n+ufkt2BnnzMZ+LdZ8+q/kH9p/5n9Z/bH75fof+U/mX7D+cPYA+RH1X+lX9m8w/6Yf0/vxagf6r+b+wF28/zv8s/dr+d/D/7v/qP4/6gdx9/wP5b+JvzP/oP0e8oTuv9M/gE/Mf/F/lv4X/Ab/v/yD/D/rV7ZflT/w/... | [{"identifier": "A", "content": "as food grade colourant\n"}, {"identifier": "B", "content": "in acid base titration as an indicatior."}, {"identifier": "C", "content": "in laboratory test for phenols"}, {"identifier": "D", "content": "in protein estimation as an alternative to ninhydrin."}] | ["B"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734263454/exam_images/ztyuoxzb3srpsiecrta4.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2020 (Online) 7th January Morning Slot Chemistry - Compounds Containing Nitrogen Question 156 English Explanatio... | mcq | jee-main-2020-online-7th-january-morning-slot | 1,345 |
J7XhJynYKhO6Kt8U3c7k9k2k5ll7yd1 | chemistry | compounds-containing-nitrogen | aromatic-amines | The decreasing order of basicity of the
following amines is :
<img src="data:image/png;base64,UklGRkwHAABXRUJQVlA4IEAHAABQMQCdASreAOkAPm0yl0kkIqehIXOZePANiWlu4XNBG/Nj8Yf0b8UPBn+4fkd11XjT2Z3QH+A7cL2/+I/0jzr/1H8X8U/bjkS/qH8S/k3+c88n6AfznvCcRf4H+bf1P9cPlC9o/0H8A/YD3T7br8qvWe8GGNz/Vfzn05v7j+H/y793Pa/80/87+Hf1P5G/1A/0/8e/p/... | [{"identifier": "A", "content": "(III) > (II) > (I) > (IV)"}, {"identifier": "B", "content": "(I) > (III) > (IV) > (II)"}, {"identifier": "C", "content": "(III) > (I) > (II) > (IV)"}, {"identifier": "D", "content": "(II) > (III) > (IV) > (I)"}] | ["A"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734264887/exam_images/dmnjpe63dfdr7hxw7wyi.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2020 (Online) 9th January Evening Slot Chemistry - Compounds Containing Nitrogen Question 151 English Explanatio... | mcq | jee-main-2020-online-9th-january-evening-slot | 1,346 |
0R4b2NlAgBuAi8shPnjgy2xukf25phlh | chemistry | compounds-containing-nitrogen | aromatic-amines | The Kjeldahl method of Nitrogen estimation fails for which of the following reaction products?
<img src="data:image/png;base64,UklGRrgUAABXRUJQVlA4IKwUAADwbQCdASr0Ad4APm0ylkkkIqIhIZDKeIANiWlu/C44putQzf0Y/ln5CeAf9f/rP7S+gvhP8jeynqsfzv6AdMz3Dns38q/o3/B9Kv7h/EP6T+zfor7j/47+j+wL6Z/sf8R/nP+987H+L/j39O8Emt/6NewX7l/Kv8L/Jv5n+... | [{"identifier": "A", "content": "(a), (c) and (d)"}, {"identifier": "B", "content": "(b) and (c)"}, {"identifier": "C", "content": "(c) and (d)"}, {"identifier": "D", "content": "(a) and (d)"}] | ["C"] | null | <img src="https://res.cloudinary.com/dckxllbjy/image/upload/v1734263709/exam_images/vgi3jhslvnua05nkpxnl.webp" style="max-width: 100%;height: auto;display: block;margin: 0 auto;" loading="lazy" alt="JEE Main 2020 (Online) 3rd September Morning Slot Chemistry - Compounds Containing Nitrogen Question 149 English Explanat... | mcq | jee-main-2020-online-3rd-september-morning-slot | 1,347 |
KfpWZam4pbxLkBtIVXjgy2xukfjbr0ts | chemistry | compounds-containing-nitrogen | aromatic-amines | The increasing order of basicity of the following
compounds is :
<img src="data:image/png;base64,UklGRo4TAABXRUJQVlA4IIITAADQZwCdASrYAbgAPm02lkikIqIhIlFKuIANiWlu/HyXgCvnZ11/ol/J/x+7/v6h+Vv9i8jHzP9c/qP7Lf1b1v/4D+G/ynrc/2b+Aeaz6ifb/4x/Kf+T/gP21+Bf8F/Ev6r5u/CL+Z9Qv1b/b/4v/Rf+X/hPTh/p/5F/KO9irl/xf4b/UfcC7tf3r+R/zH/i+WX+r/w... | [{"identifier": "A", "content": "(A) < (B) < (C) < (D)"}, {"identifier": "B", "content": "(B) < (A) < (C) < (D)"}, {"identifier": "C", "content": "(D) < (A) < (B) < (C)"}, {"identifier": "D", "content": "(B) < (A) < (D) < (C)"}] | ["D"] | null | The compound which can donate lone pair more easily is more basic.
<br><br>(A) N is sp<sup>2</sup> hybridized and lone pair is localised means not perticipating in resonance.
<br><br>(B) Here lone pair perticipates in resonance and involved in aromaticity. So this is weakest base.
<br><br>(C) N is sp<sup>3</sup> hybrid... | mcq | jee-main-2020-online-5th-september-morning-slot | 1,348 |
YgAdeyDA3KJZzCHRk91klrf5wgq | chemistry | compounds-containing-nitrogen | aromatic-amines | In the following reaction the reason why meta-nitro product also formed is :<br/><br/>
<img src="data:image/png;base64,UklGRmYWAABXRUJQVlA4IFoWAADwIAGdASrKAgADP4G+2GY2L6ynITIJSsAwCWlu8mJdiqr57Vs0vDzT/v/71/ffJpq5uEOnOny7VfnQouuCPPvnxyR+j7H9sjINxECLRq24zjS+wBQPbW+1y7kOLO/PtYZXvOrCEcz1mZGIKIZX+dagvqv2j1ic5lBdExkCnIZlpJExA... | [{"identifier": "A", "content": "\u2013NH<sub>2</sub> group is highly meta-directive"}, {"identifier": "B", "content": "\u2013NO<sub>2</sub> substitution always takes place at meta-position"}, {"identifier": "C", "content": "Formation of anilinium ion"}, {"identifier": "D", "content": "low temperature"}] | ["C"] | null | Aniline on protonation forms anilinium ion, which is
meta-directing. So, a considerable amount of meta product is formed
alongwith o-nitroaniline and p-nitroaniline.
<br><br><img src="https://app-content.cdn.examgoal.net/fly/@width/image/1kxhdusb7/b239e76d-d9b8-4577-90d3-5352880c86c2/79af2230-6310-11ec-b36d-0fa4fbfb1e3... | mcq | jee-main-2021-online-24th-february-morning-slot | 1,349 |
ki2P1eTZ4qVHrz8OSC1klrvq55u | chemistry | compounds-containing-nitrogen | aromatic-amines | The total number of amines among the following which can be synthesized by Gabriel synthesis is __________.<br/><br/><img src="data:image/png;base64,UklGRjQRAABXRUJQVlA4ICgRAADw9wCdASpcAgADP4HA22W2MK2nIhIZEsAwCWlu4XNBG/Pn9D/7H1ZdRvLHWB4m2cHbL8x/vX1s9483/571TbK0x5L//8C0OYs7eMYyKqEzd3FnfKKXuLO+UUvcWd8kRHvNMaxrdiAbmajazyV... | [] | null | 3 | <p>Gabriel phthalimide synthesis is used to prepare 1<sup>o</sup> aliphatic or alicyclic amine. Hence, amine which can be synthesised by Gabriel phthalimide synthesis method contains $$\alpha $$-carbon.</p>
<p>Aniline (C<sub>6</sub>H<sub>5</sub>NH<sub>2</sub>) does not contain $$\alpha $$-C cannot be prepared by Gabrie... | integer | jee-main-2021-online-24th-february-evening-slot | 1,350 |
OQLKCrFpifIF1WUlhA1klsblv1b | chemistry | compounds-containing-nitrogen | aromatic-amines | Which of the following reaction/s will not give p-aminoazobenzene?<br/><br/><img src="data:image/png;base64,UklGRngaAABXRUJQVlA4IGwaAACQdACdASoMATcBPm00lkikIqIhJDI6sIANiWlu/HyYdl9ZMo6rwz/JPxZ8x36J/Zf7h+xvn/+L/Lf2f8ofVV/tekx+MfVn+U/WX7n/H/7t/tv7d+8Xwz/ov49+0nnH72v6/+k+wL6n/wP8g/s3/Z/xHpe/s38Y/s363+MzsX9N/ST2AvY/5V/hf4//... | [{"identifier": "A", "content": "C only "}, {"identifier": "B", "content": "A only "}, {"identifier": "C", "content": "A and B"}, {"identifier": "D", "content": "B only"}] | ["D"] | null | <picture><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734263767/exam_images/qvvkf6vm55s3vw0qznfb.webp"><source media="(max-width: 500px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734265116/exam_images/devnodrgzfsqo7jhi6bf.webp"><source media="(max-wid... | mcq | jee-main-2021-online-25th-february-morning-slot | 1,351 |
kVSPeXxIAApR5Q2Lqa1kltbfgba | chemistry | compounds-containing-nitrogen | aromatic-amines | <img src="data:image/png;base64,UklGRrIRAABXRUJQVlA4IKYRAACwXgCdASr0AZUAPm00lkikIqIhIvGquIANiWlu/HyYEsgeh+ipTdBV+F/5b+PXmM/Tv69+Tf9k9R/xf51+y/kfuON8P+b/ln9h/5n9h+cf5n/mP5N/WP1s9G/fZ/Yfxj+ge4L6n/wP8l/o3/I/t3qM/3P8Z/m3g1Vj/T32BfbP5d/pv5X/Wv1k87n+D/mv9u/5P9O+CvrR/bPs5+wP9Tv9T/Hf69/0/ir/F/o3/RfOu8J/UD4Bv6H/UP8b/I/7r+wHwCf3... | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734265965/exam_images/zudjjmkabmgeln4jh5my.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2021 (Online) 25th February Evening Shift Chemistry - Compounds Containi... | ["C"] | null | <picture><source media="(max-width: 889px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267406/exam_images/zpudwjf8urani7fg2r5a.webp"><source media="(max-width: 320px)" srcset="https://res.cloudinary.com/dckxllbjy/image/upload/v1734267500/exam_images/tdc2gvnxlaubyk9psbd6.webp"><source media="(max-wid... | mcq | jee-main-2021-online-25th-february-evening-slot | 1,352 |
NReYmPyrooo4Ow5dgV1klurhdy6 | chemistry | compounds-containing-nitrogen | aromatic-amines | A. Phenyl methanamine<br/><br/>B. N,N-Dimethylaniline<br/><br/>C. N-Methyl aniline<br/><br/>D. Benzenamine<br/><br/>Choose the correct order of basic nature of the above amines. | [{"identifier": "A", "content": "D > C > B > A"}, {"identifier": "B", "content": "A > C > B > D"}, {"identifier": "C", "content": "D > B > C > A"}, {"identifier": "D", "content": "A > B > C > D"}] | ["D"] | null | <p>In phenyl methanamine, the lone pair on nitrogen of -NH<sub>2</sub>
group is localised and does not undergoes resonance.
</p>
<img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l45tmmxy/b672242b-b509-4733-a7db-595f983265b1/44fd7460-e74a-11ec-885c-21e515ff74ea/file-1l45tmmxz.png?format=png" data-orsrc=... | mcq | jee-main-2021-online-26th-february-evening-slot | 1,354 |
d4FaJ5Ftcr2BmdeFjo1kmm0fgi5 | chemistry | compounds-containing-nitrogen | aromatic-amines | <img src="data:image/png;base64,UklGRpoWAABXRUJQVlA4II4WAABQcwCdASqUArAAPm0wlkkkIqIhItDaEIANiWlu/H+P6ZV0/xNFz/0a/h/5O+C39m/sf7O+hP4l84/XvyJ9Vv4l89fRP+N/gHdU+4/xf+s/8/06/wX8U/bT+j+h/vO/g/UF/KP4t/Xf5R/XP+Z/e/hh9t/0f8i/sfhQ55/gP9l/MPYF9pPmP96/kX9c/5f+D8/X95/hH9Y/1vuh9X/9p/KfgA/Uj/OfyL+4/779////93/8P/geLf5t7Af8//on91/kf92/... | [{"identifier": "A", "content": "B > C > A"}, {"identifier": "B", "content": "A > C > B"}, {"identifier": "C", "content": "C > A > B"}, {"identifier": "D", "content": "C > B > A"}] | ["D"] | null | During nitration of aniline, meta-nitroaniline is also formed as
product due to formation of NH<sub>3</sub><sup>+</sup>
group which is meta directing
group under strongly acidic medium. The percentage of p, m and o
product is 51%, 47% and 2%, respectively.
<br><br><img src="https://app-content.cdn.examgoal.net/fly/@wid... | mcq | jee-main-2021-online-18th-march-evening-shift | 1,356 |
1krq53kp5 | chemistry | compounds-containing-nitrogen | aromatic-amines | The correct structure of Rhumann's Purple, the compound formed in the reaction of ninhydrin with proteins is : | [{"identifier": "A", "content": "<img src=\"https://res.cloudinary.com/dckxllbjy/image/upload/v1734265593/exam_images/dpx3lrvb3a3cmkb4alc9.webp\" style=\"max-width: 100%;height: auto;display: block;margin: 0 auto;\" loading=\"lazy\" alt=\"JEE Main 2021 (Online) 20th July Morning Shift Chemistry - Compounds Containing N... | ["D"] | null | <p>Rhumann’s purple is confirmatory test for the presence of protein. The correct structure of Rhumann’s Purple, the compound formed in the reaction of ninhydrin with proteins is an follows</p>
<img src="https://app-content.cdn.examgoal.net/fly/@width/image/1l2o3010z/3c9941ba-0050-4d55-b324-d06026071c87/987b8830-c9bc-1... | mcq | jee-main-2021-online-20th-july-morning-shift | 1,357 |
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