All the steps involved in the acid-catalyzed reaction of an imine with water to yield an aldehyde or ketone along with a primary amine are to be shown. Concept introduction: Primary amines react with aldehydes and ketones to yield imines R 2 C=NR. The reaction is reversible in nature. The attack of water on the protonated imine and subsequent deprotonation yield a carbinolamine intermediate. The intermediate on further reaction breaks to yield a ketone and amine as products. To show: All the steps involved in the acid-catalyzed reaction of an imine with water to yield an aldehyde or ketone along with a primary amine.

Question

Want to see the full answer?

Answer 1

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 19.8, Problem 11P

Interpretation Introduction

Interpretation:

All the steps involved in the acid-catalyzed reaction of an imine with water to yield an aldehyde or ketone along with a primary amine are to be shown.

Concept introduction:

Primary amines react with aldehydes and ketones to yield imines R₂C=NR. The reaction is reversible in nature. The attack of water on the protonated imine and subsequent deprotonation yield a carbinolamine intermediate. The intermediate on further reaction breaks to yield a ketone and amine as products.

To show:

All the steps involved in the acid-catalyzed reaction of an imine with water to yield an aldehyde or ketone along with a primary amine.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

I'm trying to memorize VESPR Shapes to solve problems like those. I need help making circles like the second image in blue or using an x- and y-axis plane to memorize these and solve those types of problems, especially the ones given in the top/first image (180, 120, 109.5). Can you help me with this? or is their any other efficient method do so

Can you please explain this problems to me? I'm very confused about it. Please provide a detailed, step-by-step explanation for me! (ME EX1) Prblm 27

Question 6 of 7 (1 point) | Question Attempt: 1 of 1 = 1 ✓2 ✓ 3 ✓ 4 ✓ 5 6 ✓ 7 This organic molecule is dissolved in a basic aqueous solution: Jen ✓ ? A short time later sensitive infrared spectroscopy reveals the presence of a new C-OH stretch absorption. That is, must now be a new molecule present with at least one C- OH bond. there 18 In the drawing area below, show the detailed mechanism that could convert the molecule above into the new molecule Ar © + Click and drag to start drawing a structure. Add/Remove step Click and drawing Save For Later Submit Assignment

Answer 2

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 19.8, Problem 11P

Interpretation Introduction

Interpretation:

All the steps involved in the acid-catalyzed reaction of an imine with water to yield an aldehyde or ketone along with a primary amine are to be shown.

Concept introduction:

Primary amines react with aldehydes and ketones to yield imines R₂C=NR. The reaction is reversible in nature. The attack of water on the protonated imine and subsequent deprotonation yield a carbinolamine intermediate. The intermediate on further reaction breaks to yield a ketone and amine as products.

To show:

All the steps involved in the acid-catalyzed reaction of an imine with water to yield an aldehyde or ketone along with a primary amine.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 19.8, Problem 11P

Interpretation Introduction

Interpretation:

All the steps involved in the acid-catalyzed reaction of an imine with water to yield an aldehyde or ketone along with a primary amine are to be shown.

Concept introduction:

Primary amines react with aldehydes and ketones to yield imines R₂C=NR. The reaction is reversible in nature. The attack of water on the protonated imine and subsequent deprotonation yield a carbinolamine intermediate. The intermediate on further reaction breaks to yield a ketone and amine as products.

To show:

All the steps involved in the acid-catalyzed reaction of an imine with water to yield an aldehyde or ketone along with a primary amine.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

Chapter 19.8, Problem 11P

Interpretation Introduction