Chapter 5: Q. 30 E-b (page 148)
Orient each of the following drawings so that the lowest-ranked group is toward the rear, and then assign R or S configuration
Short Answer
(b). R configuration
Chapter 5: Q. 30 E-b (page 148)
Orient each of the following drawings so that the lowest-ranked group is toward the rear, and then assign R or S configuration
(b). R configuration
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Get started for freeKetones react with sodium acetylide (the sodium salt of acetylene,) to give alcohols. For example, the reaction of sodium acetylide with 2-butanone yields 3-methyl-1-pentyn-3-ol
(a)Is the product chiral?
(b)Assuming that the reaction takes place with equal likelihood from both Reand Sifaces of the carbonyl group, is the product optically active? Explain.
The first step in the metabolism of glycerol, formed by digestion of fats, is phosphorylation of the pro-R group by reaction with adenosine triphosphate (ATP) to give the corresponding glycerol phosphate plus adenosine diphosphate (ADP). Show the stereochemistry of the product.
How many stereoisomers of 2,4-dibromo-3-chloropentane are there? Draw them, and indicate which are optically active.
Which of the following objects are chiral?
(a) A basketball
(b) A fork
(c) A wine glass
(d) A golf club
(e) A spiral staircase
(f) A snowflake
(e)
Assign R or S configuration to each chirality center in pseudoephedrine, an over-the-counter decongestant found in cold remedies (blue = N)
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