Biochemistry
6th Edition
ISBN: 9781305577206
Author: Reginald H. Garrett, Charles M. Grisham
Publisher: Cengage Learning
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Textbook Question
Chapter 3, Problem 2P
Answers to all problems are at the end of this book. Detailed solutions are available in the Student Solutions Manual, Study Guide, and Problems Book.
Calculating
The equilibrium constant for some process
Why- is it important in this problem to assume that
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Show the fate of the hydrogen on carbon-2 of glucose.
Please draw out the structure using curve arrows to show electron flow.
3. Which one of the compounds
below is the major product formed by
the reaction sequence shown here?
CH3 +
CH3NO2
NaOH
H2, Ni
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nitromethane
acetophenone
OH
OH
HO HN-
u x x x x
Ph
A
HO
-NH2
HO
H
Ph
Ph
Ph
N-
H
B
Ph
NH2
D
E
4. Only ONE of the five compounds below can be prepared by an aldol condensation in
which a single carbonyl compound is treated with base. Which one is it?
To solve this problem, reverse the aldol condensation that formed each of these molecules to find out what two molecules
came together to make the products. The one in which the two molecules are identical is the answer.
Ph
Ph
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A
Ph
H
B
Ph
Ph
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Ph.
Ph
Ph
E
H
Chapter 3 Solutions
Biochemistry
Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at (he end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Prob. 9PCh. 3 - Answers to all problems are at the end of this...
Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...Ch. 3 - Answers to all problems are at the end of this...
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- 5. Which one is the major organic product obtained from the following reaction sequence? First, equimolar amounts of cyclopentanone and LDA are mixed at -78°C. Then propionaldehyde (propanal) is added. Addition of aqueous acid completes the process. LDA, -78°C. 1. 2. H₂O* H A B H 0 D H H Earrow_forward2. Which one is the major organic product obtained from the following reaction? NaOH, H₂O heat A B C D Earrow_forwardCH3CH2CHO + propanal PhCH2CHO 2-phenylacetaldehyde mixture of four products NaOH 10. In the crossed aldol reaction of propanal and 2-phenylacetaldehyde shown above, a mixture of four products will be formed. Which ONE of the compounds below will NOT be formed in this crossed aldol reaction? OH Ph A H OH OH Ph H B OH OH H H H Ph Ph C Ph D Earrow_forward
- An organic chemist ordered the wrong item. She wanted to obtain 1-hydroxy-2-butanone, butinstead ordered 2-hydroxybutyraldehyde. As a good biochemist, show how the organic chemistcould use biological catalysis to make her desired compound.arrow_forwardPredict the products of aldolase catalyzing the reaction with acetone and (S)-3-hydroxybutyraldehyde.arrow_forwardA cancer patient undergoing chemotherapy is taking a protein kinase inhibitor drug. The patientis an avid marathon runner and does not want to miss his upcoming race. Is it a good idea forthis patient to attempt a marathon while on this medication? Explain why or why not.arrow_forward
- Show the fate of the hydrogen on carbon-2 of glucose.arrow_forwardImagine that aldolase can react with the seven carbon molecule Sedoheptulose-1,7-bisphosphate (below). Use the mechanism to predict the two products generated.arrow_forwardShow the mechanisms of PGK and PFK-1. How are they different?arrow_forward
- Show the fate of the proton on the 4-Oxygen molecule of F-1,6-BP.arrow_forwardSodium borohydride (NaBH4) is a potent inhibitor of aldolase. It is known to ONLY inhibit theenzyme when it is complexed with substrate. Treatment of the enzyme alone has no effect.What is the mechanism for this inhibition?arrow_forwardA non-hydrolysable ATP (AMPPNP - below) is ingested by a graduate student on a dare. Whateffects would you anticipate on his metabolism?arrow_forward
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