Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Circle the letter next to the most appropriate response. 1) Which is likely to be the least soluble with water? a) hexane b) acetone c) trichloromethane d) trinitro-toluene 2) Which is likely to be the most soluble in 3,4-dimethyloctane? a) hexane b) acetone c) trichloromethane d) trinitro-toluene 3) When ammonium nitrate is dissolved in water, the solution: a) gets warmer. b) gets colder. c) stays the same temperature. d) is none of the above because potassium nitrate is insoluble.

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Answer 2

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Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Answer 3

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Expert Solution & Answer

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Answer 4

Question

Definition Definition Organic compounds that have a carbonyl group, C = O, as their functional group. The carbonyl group in ketones is placed somewhere in the middle of the molecular structure, which means, the C=O is attached to two alkyl groups or benzene rings. Just like all other homologous series, the naming of ketones is done using a common suffix “-one”. The general molecular formula is C n H 2n O. Functional group of a ketone

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Expert Solution & Answer

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Answer 5

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Answer 6

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Answer 7

Chapter 29.SE, Problem 54AP

Interpretation Introduction

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Answer 8

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Answer 9

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Answer 11

Ch. 29.1 - Prob. 1P Ch. 29.3 - Write the equations for the remaining passages of...Ch. 29.3 - Prob. 3P Ch. 29.4 - Write a mechanism for the dehydration reaction of...Ch. 29.4 - Evidence for the role of acetate in fatty-acid...Ch. 29.4 - Does the reduction of acetoacetyl ACP in step 6...Ch. 29.5 - Prob. 7P Ch. 29.5 - Look at the entire glycolysis pathway, and make a...Ch. 29.6 - Prob. 9P Ch. 29.7 - Prob. 10P

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Solution Summary: The author explains that hydride ion adds to the Si face or the Re face of acetoacetyl ACP, a prochiral concept of addition.

Concept explainers

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

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Chapter 29 Solutions

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Solution Summary: The author explains that hydride ion adds to the Si face or the Re face of acetoacetyl ACP, a prochiral concept of addition.

Concept explainers

Interpretation: Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.

Want to see the full answer?

Chapter 29 Solutions

Interpretation:

Fatty-acid biosynthesis (Figure 29-5), acetoacetyl ACP is reduced stereospecifically by NADPH to yield an alcohol and explain hydride ion add to the Si face or the Re face of acetoacetyl ACP.