ethylamine NABH,CN H;C One problem with reductive amination as a method of amine synthesis, is that by-products are sometimes obtained. For example, reductive zmination of benzaldehyde with ethylamine leads to the expected product, N-ethylbenzylamine However, significant amounts of N-methyldibenzylamine are also recovered. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism leading to the by-product. Arrow-pushing Instructions H-A он `H `NH2 :A CH3 `CH3

Organic Chemistry
9th Edition
ISBN:9781305080485
Author:John E. McMurry
Publisher:John E. McMurry
Chapter24: Amines And Heterocycles
Section24.SE: Something Extra
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ethylamine
NABH,CN
One problem with reductive amination as a method of amine synthesis, is that by-products are sometimes obtained. For example, reductive zmination of benzaldehyde with ethylamine leads to
the expected product, N-ethylbenzylamine However, significant amounts of N-methyldibenzylamine are also recovered.
Draw curved arrows to show the movement of electrons in this step of the reaction mechanism leading to the by-product.
Arrow-pushing Instructions
H-A
OH
`H
NH2
:A
CH3
`CH3
Transcribed Image Text:ethylamine NABH,CN One problem with reductive amination as a method of amine synthesis, is that by-products are sometimes obtained. For example, reductive zmination of benzaldehyde with ethylamine leads to the expected product, N-ethylbenzylamine However, significant amounts of N-methyldibenzylamine are also recovered. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism leading to the by-product. Arrow-pushing Instructions H-A OH `H NH2 :A CH3 `CH3
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