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A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. 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 A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. Can you explain this answer? covers all topics & solutions for Chemistry 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. Can you explain this answer?.

Solutions for A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. Can you explain this answer? in English & in Hindi are available as part of our courses for Chemistry. Download more important topics, notes, lectures and mock test series for Chemistry Exam by signing up for free.

Here you can find the meaning of A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. Can you explain this answer?, a detailed solution for A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. Can you explain this answer? has been provided alongside types of A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice A C5H12O2 compound has strong infrared absorption at 3300 to 3400cm-1. The 1H NMR spectrum has three singlets at β 0.9, β 3.45 and β 3.2 ppm with relative areas 3:2:1. Addition of D2O to the sample eliminates the lower field signal. The 13C NMR spectrum shows three signals all at higher field than β 100 ppm. Which of the following compounds best fits this data:a)1, 5-pentanediolb)1, 3-dimethoxypropanec)2, 2-dimethyl-1, 3-propanediold)2, 4-pentanediolCorrect answer is option 'C'. Can you explain this answer? tests, examples and also practice Chemistry tests.