A complete and detailed mechanism for the reactions in Equation 18 − 15 is to be drawn. Concept introduction: If an aldehyde or ketone is treated with a large excess of an alcohol under acidic conditions, then the hemiacetal produced from nucleophilic addition reacts further to form an acetal, in which two alkoxy ( RO ) groups are bonded to the same carbon. The complete mechanism for this acetal formation reaction is shown in Equation 18 − 13 : The equation 18 − 15 is: The reversibility of acetal formation enables us to use acetals as protecting groups for ketones and aldehydes . Ketones and aldehydes are susceptible to an attack by nucleophiles (at the carbonyl carbon) and bases (at the α carbon), but acetals are inert to both strong nucleophiles and strong bases. One popular alcohol used to protect ketones and aldehydes is 1 , 2 − ethanediol (ethylene glycol), as shown in Equation 18 − 15 . 1 , 2 − ethanediol has two OH functional groups per molecule, so only one equivalent of the diol is needed. It also forms a five membered ring, which helps favor acetal formation.

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Answer 1

Question

Chapter 18, Problem 18.8P

Interpretation Introduction

Interpretation:

A complete and detailed mechanism for the reactions in Equation 18−15 is to be drawn.

Concept introduction:

If an aldehyde or ketone is treated with a large excess of an alcohol under acidic conditions, then the hemiacetal produced from nucleophilic addition reacts further to form an acetal, in which two alkoxy (RO) groups are bonded to the same carbon. The complete mechanism for this acetal formation reaction is shown in Equation 18−13:

The equation 18−15 is:

The reversibility of acetal formation enables us to use acetals as protecting groups for ketones and aldehydes. Ketones and aldehydes are susceptible to an attack by nucleophiles (at the carbonyl carbon) and bases (at the α carbon), but acetals are inert to both strong nucleophiles and strong bases. One popular alcohol used to protect ketones and aldehydes is 1,2−ethanediol (ethylene glycol), as shown in Equation 18−15. 1,2−ethanediol has two OH functional groups per molecule, so only one equivalent of the diol is needed. It also forms a five membered ring, which helps favor acetal formation.

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Answer 2

Question

Chapter 18, Problem 18.8P

Interpretation Introduction

Interpretation:

A complete and detailed mechanism for the reactions in Equation 18−15 is to be drawn.

Concept introduction:

If an aldehyde or ketone is treated with a large excess of an alcohol under acidic conditions, then the hemiacetal produced from nucleophilic addition reacts further to form an acetal, in which two alkoxy (RO) groups are bonded to the same carbon. The complete mechanism for this acetal formation reaction is shown in Equation 18−13:

The equation 18−15 is:

The reversibility of acetal formation enables us to use acetals as protecting groups for ketones and aldehydes. Ketones and aldehydes are susceptible to an attack by nucleophiles (at the carbonyl carbon) and bases (at the α carbon), but acetals are inert to both strong nucleophiles and strong bases. One popular alcohol used to protect ketones and aldehydes is 1,2−ethanediol (ethylene glycol), as shown in Equation 18−15. 1,2−ethanediol has two OH functional groups per molecule, so only one equivalent of the diol is needed. It also forms a five membered ring, which helps favor acetal formation.

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Answer 3

Question

Chapter 18, Problem 18.8P

Interpretation Introduction

Interpretation:

A complete and detailed mechanism for the reactions in Equation 18−15 is to be drawn.

Concept introduction:

If an aldehyde or ketone is treated with a large excess of an alcohol under acidic conditions, then the hemiacetal produced from nucleophilic addition reacts further to form an acetal, in which two alkoxy (RO) groups are bonded to the same carbon. The complete mechanism for this acetal formation reaction is shown in Equation 18−13:

The equation 18−15 is:

The reversibility of acetal formation enables us to use acetals as protecting groups for ketones and aldehydes. Ketones and aldehydes are susceptible to an attack by nucleophiles (at the carbonyl carbon) and bases (at the α carbon), but acetals are inert to both strong nucleophiles and strong bases. One popular alcohol used to protect ketones and aldehydes is 1,2−ethanediol (ethylene glycol), as shown in Equation 18−15. 1,2−ethanediol has two OH functional groups per molecule, so only one equivalent of the diol is needed. It also forms a five membered ring, which helps favor acetal formation.

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Answer 4

Question

Chapter 18, Problem 18.8P

Interpretation Introduction

Interpretation:

A complete and detailed mechanism for the reactions in Equation 18−15 is to be drawn.

Concept introduction:

If an aldehyde or ketone is treated with a large excess of an alcohol under acidic conditions, then the hemiacetal produced from nucleophilic addition reacts further to form an acetal, in which two alkoxy (RO) groups are bonded to the same carbon. The complete mechanism for this acetal formation reaction is shown in Equation 18−13:

The equation 18−15 is:

The reversibility of acetal formation enables us to use acetals as protecting groups for ketones and aldehydes. Ketones and aldehydes are susceptible to an attack by nucleophiles (at the carbonyl carbon) and bases (at the α carbon), but acetals are inert to both strong nucleophiles and strong bases. One popular alcohol used to protect ketones and aldehydes is 1,2−ethanediol (ethylene glycol), as shown in Equation 18−15. 1,2−ethanediol has two OH functional groups per molecule, so only one equivalent of the diol is needed. It also forms a five membered ring, which helps favor acetal formation.

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Answer 5

Chapter 18, Problem 18.8P

Interpretation Introduction

Interpretation:

A complete and detailed mechanism for the reactions in Equation 18−15 is to be drawn.

Concept introduction:

If an aldehyde or ketone is treated with a large excess of an alcohol under acidic conditions, then the hemiacetal produced from nucleophilic addition reacts further to form an acetal, in which two alkoxy (RO) groups are bonded to the same carbon. The complete mechanism for this acetal formation reaction is shown in Equation 18−13:

The equation 18−15 is:

The reversibility of acetal formation enables us to use acetals as protecting groups for ketones and aldehydes. Ketones and aldehydes are susceptible to an attack by nucleophiles (at the carbonyl carbon) and bases (at the α carbon), but acetals are inert to both strong nucleophiles and strong bases. One popular alcohol used to protect ketones and aldehydes is 1,2−ethanediol (ethylene glycol), as shown in Equation 18−15. 1,2−ethanediol has two OH functional groups per molecule, so only one equivalent of the diol is needed. It also forms a five membered ring, which helps favor acetal formation.

Answer 6

Chapter 18, Problem 18.8P

Interpretation Introduction

Interpretation:

A complete and detailed mechanism for the reactions in Equation 18−15 is to be drawn.

Concept introduction:

If an aldehyde or ketone is treated with a large excess of an alcohol under acidic conditions, then the hemiacetal produced from nucleophilic addition reacts further to form an acetal, in which two alkoxy (RO) groups are bonded to the same carbon. The complete mechanism for this acetal formation reaction is shown in Equation 18−13:

The equation 18−15 is:

The reversibility of acetal formation enables us to use acetals as protecting groups for ketones and aldehydes. Ketones and aldehydes are susceptible to an attack by nucleophiles (at the carbonyl carbon) and bases (at the α carbon), but acetals are inert to both strong nucleophiles and strong bases. One popular alcohol used to protect ketones and aldehydes is 1,2−ethanediol (ethylene glycol), as shown in Equation 18−15. 1,2−ethanediol has two OH functional groups per molecule, so only one equivalent of the diol is needed. It also forms a five membered ring, which helps favor acetal formation.

Answer 7

Chapter 18, Problem 18.8P

Interpretation Introduction

Interpretation:

A complete and detailed mechanism for the reactions in Equation 18−15 is to be drawn.

Concept introduction:

If an aldehyde or ketone is treated with a large excess of an alcohol under acidic conditions, then the hemiacetal produced from nucleophilic addition reacts further to form an acetal, in which two alkoxy (RO) groups are bonded to the same carbon. The complete mechanism for this acetal formation reaction is shown in Equation 18−13:

The equation 18−15 is:

The reversibility of acetal formation enables us to use acetals as protecting groups for ketones and aldehydes. Ketones and aldehydes are susceptible to an attack by nucleophiles (at the carbonyl carbon) and bases (at the α carbon), but acetals are inert to both strong nucleophiles and strong bases. One popular alcohol used to protect ketones and aldehydes is 1,2−ethanediol (ethylene glycol), as shown in Equation 18−15. 1,2−ethanediol has two OH functional groups per molecule, so only one equivalent of the diol is needed. It also forms a five membered ring, which helps favor acetal formation.

Answer 8

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Answer 11

Ch. 18 - Prob. 18.1P Ch. 18 - Prob. 18.2P Ch. 18 - Prob. 18.3P Ch. 18 - Prob. 18.4P Ch. 18 - Prob. 18.5P Ch. 18 - Prob. 18.6P Ch. 18 - Prob. 18.7P Ch. 18 - Prob. 18.8P Ch. 18 - Prob. 18.9P Ch. 18 - Prob. 18.10P

Solution Summary: The author explains the mechanism for the reaction in Equation 18-15.

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