Commercially available d-nitromethane (CHNO.) that was 99.9% deuterated was purchased and its Hand C {H} NMR spectra recorded. The H spectrum showed one 1:2:3:2:1 quintet at 4.33 p.p.m. whereas the C {H} spectrum showed a non-binomial septet at 62.8 p.p.m. Assign and explain this data.
Commercially available d-nitromethane (CHNO.) that was 99.9% deuterated was purchased and its Hand C {H} NMR spectra recorded. The H spectrum showed one 1:2:3:2:1 quintet at 4.33 p.p.m. whereas the C {H} spectrum showed a non-binomial septet at 62.8 p.p.m. Assign and explain this data.
Chapter13: Structure Determination: Nuclear Magnetic Resonance Spectroscopy
Section13.SE: Something Extra
Problem 56GP: Long-range coupling between protons more than two carbon atoms apart is sometimes observed when ...
Related questions
Question
Commercially available d-nitromethane (CHNO.) that was 99.9% deuterated was purchased and its Hand C {H} NMR spectra recorded. The H spectrum showed one 1:2:3:2:1 quintet at 4.33 p.p.m. whereas the C {H} spectrum showed a non-binomial septet at 62.8 p.p.m. Assign and explain this data.
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
Step by step
Solved in 2 steps
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Recommended textbooks for you