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An optically active primary amine C₄H₁₁N is made by the… | StemPy Lab
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An optically active primary amine C₄H₁₁N is made by the Hofmann bromamide degradation of an amide. The group on the carbonyl carbon moves to nitrogen without changing its configuration. Which amide was used?
Chemistry
Hard
High School (11–12)
Organic Compounds with Functional Groups › Amines
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StemPy Lab
An optically active primary amine
C
4
H
11
N
\text{C}_{4}\text{H}_{11}\text{N}
C
4
H
11
N
is made by the Hofmann bromamide degradation of an amide. The group on the carbonyl carbon moves to nitrogen without changing its configuration. Which amide was used?
Pentanamide
2,2-Dimethylpropanamide
3-Methylbutanamide
2-Methylbutanamide
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← How many amines of the formula C₇H₉N, primary, secondary and tertiary together, contain a benzene ring?
Statement I: trimethylamine boils at a lower temperature than propan-1-amine. Statement II: trimethylamine is much less soluble in water than propan-1-amine. Which option is correct? →
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Organic Compounds with Functional Groups › Amines
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