Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter FRP, Problem 38P

In addition to more highly fluorinated products, fluorination of 2-methylbutane yields a mixture of compounds with the formula C 5 H 11 F .

(a) How many different isomers with the formula C 5 H 11 F would you expect to be produced, taking stereochemistry into account?

(b) If the mixture of C 5 H 11 F isomers were subjected to fractions distillation, bow many fractions would you expect to obtain?

(c) Which fractions would be optically inactive?

(d) Which would you be able to resolve into enantiomers?

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For each alkane, which mono brominated derivatives could you form in good yield by free-radical bromination?(a) cyclopentane                                                   (b) methylcyclopentane(c) 2-methylpentane                                             (d) 2,2,3,3-tetramethylbutane
1. Deduce the structure of each compound from the information given. All unknowns in this problem have molecular formula C8H12. (a) Upon catalytic hydrogenation, unknown W gives cyclooctane. Ozonolysis of W, followed by reduction with dimethylsulfide, gives octanedioic acid, HOOC—(CH2)6—COOH. Draw the structure of W. (b) Upon catalytic hydrogenation, unknown X gives cyclooctane. Ozonolysis of X, followed by reduction with dimethyl sulfide, gives two equivalents of butanedial,  O=CH—CH2CH2—CH=O. Draw the structure of X.
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