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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Water production from fatty acid oxidation is a survival mechanism in animals where water is scarce. Cells oxidize palmitoyl-CoA to produce water. If an animal has 5.000 kg of palmitoyl-CoA available for fatty acid oxidation, how many kilograms of water could the animal produce from that palmitoyl-CoA? The chemical formula for palmitoyl-CoA is C37H66N7O17P3S.

H-C-U-o 27. The following is step 3 of the citric acid cycle. What is the functional transformation that occurs in the first part of this step? group COO COO NAD* NADH + H* CH2 CH2 0 H-C-C CH2 H-C-H H-C-COO- Но-с-н COO COO Isocitrate a-ketoglutarate A) A ketone and an alcohol change positions. C) The -COO is transformed. B) An alcohol becomes a ketone. D) The alcohol becomes an aldehyde. 28. The following is step 3 of the citric acid cycle. What is the identity of the Molecule represented by I? COO COO NAD* NADH + H* I COO CH2 CH2 0 H-C-C CH2 H-C-H H-C-COO- HO-C-H COO COO Isocitrate a-ketoglutarate A) Acetate B) GTP C) NADH D) FADH2 E) CO2

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.

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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 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.