| [ | |
| { | |
| "id": "Perception_7eb1_250723_110558_003092_0", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_003092_0_q.png" | |
| ], | |
| "question": "Given the chemical formula C14H12O2 (C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2). Observe this H-NMR spectrum. The singlet peak around ~7.3 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group", | |
| "-OH group", | |
| "Aromatic protons" | |
| ], | |
| "answer": "Aromatic protons", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_039550_1", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_039550_1_q.png" | |
| ], | |
| "question": "Given the chemical formula C4H4N2 (C(CC#N)C#N). In this H-NMR spectrum, the singlet peak around ~2.0 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group (CH3)", | |
| "Methylene group (CH2)", | |
| "Nitrile group (C#N)", | |
| "Aromatic protons" | |
| ], | |
| "answer": "Methylene group (CH2)", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_068340_2", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_068340_2_q.png" | |
| ], | |
| "question": "Given the SMILES CC1=CC(=C(C(=C1)C)C). In this HNMR spectrum, the singlet peak around ~1.5 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Terminal methyl group (CH3)", | |
| "Methine group (CH)", | |
| "Methylene group (CH2)", | |
| "Aromatic protons" | |
| ], | |
| "answer": "Terminal methyl group (CH3)", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_094602_3", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_094602_3_q.png" | |
| ], | |
| "question": "Given the chemical formula C9H11Br. Observe this H-NMR spectrum. The triplet peak around ~4.3 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Aromatic protons", | |
| "Protons adjacent to Br", | |
| "-CH3 group", | |
| "Protons on the double bond" | |
| ], | |
| "answer": "Protons adjacent to Br", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_126148_4", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_126148_4_q.png" | |
| ], | |
| "question": "Given the chemical formula C10H7Cl (C1=CC=C2C=C(C=CC2=C1)Cl). Observe this HNMR spectrum. The singlet peak around ~6.8 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Aromatic CH adjacent to Cl", | |
| "Aromatic CH next to a double bond", | |
| "Aliphatic CH3 group", | |
| "CH2 group" | |
| ], | |
| "answer": "Aromatic CH next to a double bond", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_159010_5", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_159010_5_q.png" | |
| ], | |
| "question": "Given the chemical formula C9H8O (C1CC(=O)C2=CC=CC=C21). Observe this H-NMR spectrum. The singlet peak around ~7.5 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group", | |
| "Methylene group", | |
| "Aromatic protons", | |
| "Keto proton" | |
| ], | |
| "answer": "Aromatic protons", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_222397_7", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_222397_7_q.png" | |
| ], | |
| "question": "Given the chemical formula C6H10O3 (CC1(CCOC(=O)C1)O). Observe this H-NMR spectrum. The quartet peak around ~3.5 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group", | |
| "-OH group", | |
| "Aromatic ring" | |
| ], | |
| "answer": "-CH2 group", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_290416_9", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_290416_9_q.png" | |
| ], | |
| "question": "Given the chemical formula C4H8O3 (CCOC(=O)CO), observe this H-NMR spectrum. The quartet peak around ~4.1 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group adjacent to O", | |
| "-OH group", | |
| "Carbonyl adjacent protons" | |
| ], | |
| "answer": "-CH2 group adjacent to O", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_507008_11", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_507008_11_q.png" | |
| ], | |
| "question": "Given the chemical formula C5H4O3, observe this H-NMR spectrum. The singlet peak around ~7.3 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Aromatic hydrogen", | |
| "Methoxy hydrogen", | |
| "Aldehyde hydrogen", | |
| "Hydroxyl hydrogen" | |
| ], | |
| "answer": "Aromatic hydrogen", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_611310_14", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_611310_14_q.png" | |
| ], | |
| "question": "Given the chemical formula C8H14O4. Observe this H-NMR spectrum. The singlet peak around ~3.5 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group", | |
| "-OCH3 group", | |
| "Aromatic proton" | |
| ], | |
| "answer": "-OCH3 group", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_662131_16", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_662131_16_q.png" | |
| ], | |
| "question": "Given the chemical formula C6H11ClO2 (CC(=O)OCCCCCl). Observe this H-NMR spectrum. The triplet peak around ~1.6 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group adjacent to Cl", | |
| "-CH2 group adjacent to carbonyl", | |
| "Aromatic protons" | |
| ], | |
| "answer": "-CH2 group adjacent to Cl", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_694071_17", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_694071_17_q.png" | |
| ], | |
| "question": "Given the chemical formula C10H16, observe this H-NMR spectrum. The quartet peak around ~1.4 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group", | |
| "-CH group", | |
| "Aromatic protons" | |
| ], | |
| "answer": "-CH2 group", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_838733_18", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_838733_18_q.png" | |
| ], | |
| "question": "Given the chemical formula C6H5F. Observe this H-NMR spectrum. The singlet peak around ~7.3 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group", | |
| "Fluoro-substituted carbon", | |
| "Aromatic ring protons", | |
| "Alkene protons" | |
| ], | |
| "answer": "Aromatic ring protons", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_879220_19", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_879220_19_q.png" | |
| ], | |
| "question": "Given the chemical formula C5H4O3 (C1=COC(=C1)C(=O)O). Observe this H-NMR spectrum. The singlet peak around ~6.8 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Carboxyl hydrogen", | |
| "Aromatic hydrogen", | |
| "Methoxy hydrogen", | |
| "Alkyl hydrogen" | |
| ], | |
| "answer": "Aromatic hydrogen", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_905952_20", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_905952_20_q.png" | |
| ], | |
| "question": "Given the SMILES C1CC2=CC=CC=C2C(=O)C1. In this H-NMR spectrum, the singlet peak around ~2.6 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Proton on aromatic ring", | |
| "Proton on carbonyl group", | |
| "Proton on bridgehead carbon", | |
| "Proton on aliphatic carbon" | |
| ], | |
| "answer": "Proton on carbonyl group", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_934946_21", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_934946_21_q.png" | |
| ], | |
| "question": "Given the chemical formula C7H8O (COC1=CC=CC=C1), observe this H-NMR spectrum. The singlet peak around ~7.0 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group", | |
| "Methoxy group", | |
| "Aromatic protons", | |
| "Aldehyde proton" | |
| ], | |
| "answer": "Aromatic protons", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110558_960771_22", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110558_960771_22_q.png" | |
| ], | |
| "question": "Given the molecule C18H12 (C1=CC=C2C(=C1)C3=CC=CC=C3C4=CC=CC=C24), observe this H-NMR spectrum. The singlet peak around ~7.8 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Bridge carbon between rings", | |
| "Terminal methyl group", | |
| "Phenyl ring proton", | |
| "Methoxy group proton" | |
| ], | |
| "answer": "Phenyl ring proton", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:58" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_025906_24", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_025906_24_q.png" | |
| ], | |
| "question": "Given the chemical formula C3H4Cl2 (C=C(CCl)Cl). Observe this H-NMR spectrum. The singlet peak around ~6.0 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH2Cl group", | |
| "-CHCl group", | |
| "Vinyl proton (C=C-H)", | |
| "Aromatic ring" | |
| ], | |
| "answer": "Vinyl proton (C=C-H)", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_075821_26", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_075821_26_q.png" | |
| ], | |
| "question": "Given the chemical formula C5H9BrO2, observe this H-NMR spectrum. The triplet peak around ~1.2 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group", | |
| "-OH group", | |
| "Aromatic ring" | |
| ], | |
| "answer": "-CH2 group", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_122314_28", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_122314_28_q.png" | |
| ], | |
| "question": "Given the chemical formula C10H14O2 (C1=CC=C(C=C1)COCCCO). Observe this H-NMR spectrum. The singlet peak around ~6.9 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Aromatic protons", | |
| "Methyl protons", | |
| "Oxygen-bound protons", | |
| "Alkene protons" | |
| ], | |
| "answer": "Aromatic protons", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_152577_29", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_152577_29_q.png" | |
| ], | |
| "question": "Given the molecule C7H7Br (C1=CC=C(C=C1)CBr), observe this H-NMR spectrum. The singlet peak around ~7.4 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "The aromatic protons", | |
| "The brominated methyl group", | |
| "The methylene group", | |
| "The methyl group" | |
| ], | |
| "answer": "The aromatic protons", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_197158_31", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_197158_31_q.png" | |
| ], | |
| "question": "Given the chemical formula C10H14 (CC1=CC=C(C=C1)C(C)C). Observe this H-NMR spectrum. The singlet peak around ~6.5 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group", | |
| "Methylene group", | |
| "Aromatic protons", | |
| "Vinyl protons" | |
| ], | |
| "answer": "Aromatic protons", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_226153_32", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_226153_32_q.png" | |
| ], | |
| "question": "Given the chemical formula C12H16O2 (CC(=O)OC1=CC=C(C=C1)C(C)(C)C), observe this H-NMR spectrum. The triplet peak around ~1.2 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group (-CH3) adjacent to the aromatic ring", | |
| "Methylene group (-CH2-) connected to the carbonyl group", | |
| "Aromatic protons", | |
| "Hydroxyl group (-OH)" | |
| ], | |
| "answer": "Methyl group (-CH3) adjacent to the aromatic ring", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_250219_33", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_250219_33_q.png" | |
| ], | |
| "question": "Given the molecule with the formula C9H10O (CCC(=O)C1=CC=CC=C1). In this H-NMR spectrum, the singlet peak around ~7.2 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group", | |
| "Methylene group", | |
| "Aromatic proton", | |
| "Carbonyl proton" | |
| ], | |
| "answer": "Aromatic proton", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_275658_34", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_275658_34_q.png" | |
| ], | |
| "question": "Given the chemical formula C6H4Br2. In this H-NMR spectrum, the singlet peak around ~7.6 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group", | |
| "Aromatic protons", | |
| "Alkene protons" | |
| ], | |
| "answer": "Aromatic protons", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_295900_35", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_295900_35_q.png" | |
| ], | |
| "question": "Given the chemical formula C7H12O4. Observe this H-NMR spectrum. The singlet peak around ~1.0 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group (CH3)", | |
| "Methylene group (CH2)", | |
| "Hydroxyl group (OH)", | |
| "Aromatic proton" | |
| ], | |
| "answer": "Methyl group (CH3)", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_331662_36", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_331662_36_q.png" | |
| ], | |
| "question": "Given the chemical formula C5H14N2 (C(CCN)CCN). Observe this H-NMR spectrum. The singlet peak around ~3.0 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group adjacent to nitrogen", | |
| "-CH2 group", | |
| "-NH group", | |
| "Aromatic ring" | |
| ], | |
| "answer": "-CH3 group adjacent to nitrogen", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_390200_38", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_390200_38_q.png" | |
| ], | |
| "question": "Given the chemical formula C8H8O (C1C(O1)C2=CC=CC=C2). Observe this H-NMR spectrum. The singlet peak around ~6.8 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Protons on aromatic ring", | |
| "Protons adjacent to oxygen", | |
| "Methyl group", | |
| "Protons on carbonyl group" | |
| ], | |
| "answer": "Protons adjacent to oxygen", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_445091_40", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_445091_40_q.png" | |
| ], | |
| "question": "Given the chemical formula C6H7N (pyridine derivative). Observe the H-NMR spectrum. The singlet peak around ~8.5 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Aromatic CH", | |
| "Pyridine NH", | |
| "Alkyl CH3", | |
| "Alkyl CH2" | |
| ], | |
| "answer": "Pyridine NH", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_467091_41", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_467091_41_q.png" | |
| ], | |
| "question": "Given the SMILES CC(C1=CC=CC=C1)O. Observe this HNMR spectrum. The singlet peak around ~7.3 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group (CC)", | |
| "Phenyl ring (C1=CC=CC=C1)", | |
| "Methoxy group (O)", | |
| "Alkene group" | |
| ], | |
| "answer": "Phenyl ring (C1=CC=CC=C1)", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_497389_42", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_497389_42_q.png" | |
| ], | |
| "question": "Given the chemical formula C8H14O2. Observe this HNMR spectrum. The triplet peak around ~1.2 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group adjacent to alkene", | |
| "-CH2 group in a chain", | |
| "-OH group", | |
| "Aromatic ring" | |
| ], | |
| "answer": "-CH2 group in a chain", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_521311_43", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_521311_43_q.png" | |
| ], | |
| "question": "Given the chemical formula C6H10O (CC(=CC(=O)C)C). In this H-NMR spectrum, the singlet peak around ~1.5 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Terminal methyl group", | |
| "Methylene group", | |
| "Methyl group adjacent to carbonyl", | |
| "Alkene hydrogen" | |
| ], | |
| "answer": "Methyl group adjacent to carbonyl", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_544861_44", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_544861_44_q.png" | |
| ], | |
| "question": "Given the SMILES CC1=CC=NC=C1. Observe this H-NMR spectrum. The singlet peak around ~3.5 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group", | |
| "Proton on nitrogen", | |
| "Aromatic protons", | |
| "Vinyl protons" | |
| ], | |
| "answer": "Proton on nitrogen", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_569708_45", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_569708_45_q.png" | |
| ], | |
| "question": "Given the chemical formula C7H14O2 (CCOC(C=C)OCC). Observe this H-NMR spectrum. The triplet peak around ~4.1 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group (-CH3)", | |
| "Methylene group (-CH2-) adjacent to oxygen", | |
| "Vinyl group (C=C-H)", | |
| "Aromatic protons" | |
| ], | |
| "answer": "Methylene group (-CH2-) adjacent to oxygen", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_597096_46", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_597096_46_q.png" | |
| ], | |
| "question": "Given the chemical formula C11H16, observe this H-NMR spectrum. The singlet peak around ~2.0 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group", | |
| "Methine group", | |
| "Aromatic protons", | |
| "Protons adjacent to a carbonyl group" | |
| ], | |
| "answer": "Methine group", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_619576_47", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_619576_47_q.png" | |
| ], | |
| "question": "Given the chemical formula C5H6O (C1CC(=O)C=C1). Observe this H-NMR spectrum. The quartet peak around ~2.5 ppm in the image is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group", | |
| "-CH2 group", | |
| "-OH group", | |
| "Aromatic ring" | |
| ], | |
| "answer": "-CH2 group", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_652671_48", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_652671_48_q.png" | |
| ], | |
| "question": "Given the chemical formula C10H14 (CC(C)(C)C1=CC=CC=C1). Observe this H-NMR spectrum. The singlet peak at ~1.6 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "-CH3 group adjacent to a quaternary carbon", | |
| "-CH2 group", | |
| "-CH group in a benzene ring", | |
| "Hydroxyl group" | |
| ], | |
| "answer": "-CH3 group adjacent to a quaternary carbon", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| }, | |
| { | |
| "id": "Perception_7eb1_250723_110559_677166_49", | |
| "image_path": [ | |
| "data/Perception/Peak Assignment/Perception_7eb1_250723_110559_677166_49_q.png" | |
| ], | |
| "question": "Given the chemical formula C6H9NO5, observe this H-NMR spectrum. The singlet peak around ~2.0 ppm is most likely assigned to which part of the molecule?", | |
| "choices": [ | |
| "Methyl group", | |
| "Methylene group adjacent to carbonyl", | |
| "Amine proton", | |
| "Proton in the carboxyl group" | |
| ], | |
| "answer": "Methylene group adjacent to carbonyl", | |
| "category": "Perception", | |
| "sub_category": "Peak Assignment", | |
| "source": "", | |
| "timestamp": "2025-07-23 11:05:59" | |
| } | |
| ] |