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In the 1H NMR spectrum recorded at 293 K, an organic compound (C3H7NO), exhibited signals at 7.8 (1H, s), 2.8 (3H, s) and 2.6 (3H, s). The compound is:
  • a)
  • b)
  • c)
  • d)
Correct answer is option 'A'. Can you explain this answer?
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In the 1H NMR spectrum recorded at 293 K, an organic compound (C3H7NO)...
C should be right answer. N-H proton behave like oh proton and will not couple . whereas if this was aldehyde then it should come at 9 to 10 ppm. Again two methyl shifts would be equivalent
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In the 1H NMR spectrum recorded at 293 K, an organic compound (C3H7NO)...
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In the 1H NMR spectrum recorded at 293 K, an organic compound (C3H7NO), exhibited signals at 7.8 (1H, s), 2.8 (3H, s) and 2.6 (3H, s). The compound is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer?
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In the 1H NMR spectrum recorded at 293 K, an organic compound (C3H7NO), exhibited signals at 7.8 (1H, s), 2.8 (3H, s) and 2.6 (3H, s). The compound is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? for Chemistry 2024 is part of Chemistry preparation. The Question and answers have been prepared according to the Chemistry exam syllabus. Information about In the 1H NMR spectrum recorded at 293 K, an organic compound (C3H7NO), exhibited signals at 7.8 (1H, s), 2.8 (3H, s) and 2.6 (3H, s). The compound is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer? covers all topics & solutions for Chemistry 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for In the 1H NMR spectrum recorded at 293 K, an organic compound (C3H7NO), exhibited signals at 7.8 (1H, s), 2.8 (3H, s) and 2.6 (3H, s). The compound is:a)b)c)d)Correct answer is option 'A'. Can you explain this answer?.
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