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 6, Problem 2LGP

Consider the following sequence of reactions, taken from the early steps in a synthesis of ?-fluorooleic acid, a toxic natural compound from an African shrub. (?-Fluorooleic acid, also called “ratsbane,” has been used to kill rats and also as an arrow poison in tribal warfare. Two more steps beyond those below are required to complete its synthesis.)

(i) 1-Bromo-8-fluorooctane+sodium acetylide (the sodium salt of ethyne) compound A ( C 10 H 17 F )

(ii) Compound A + N a N H 2 compound B ( C 10 H 16 F N a )

(iii) Compound B + I ( C H 2 ) 7 C I compound C ( C 17 H 30 C I F )

(iv) Compound C + N a C N compound D ( C 18 H 30 N F )

(a) Elucidate the structures of compounds A, B, C, and D above.

(b) Write the mechanism for each of the reactions above.

(c) Write the structure of the transition state for each reaction.

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6. Provide the structures of the starting materials A to F that would produce the indicated reaction product when treated with the reagent(s) and/or catalyst(s) shown. (a) to A + B HCI (cat.) (b) KMNO4, H20 OH
Acid-catalyzed dehydration of 2,2-dimethyl-1-hexanol gave a number of isomeric alkenes including 2-methyl-2-heptene as shown in the following equation.(a) Write a stepwise mechanism for the formation of 2-methyl-2-heptene, using curved arrows to show the flow of electrons. (b) What other alkenes do you think are formed in this reaction?
4.  identify the structure of A and B in the following synthetic scheme: Write out complete reactions for each step, showing the structure of all reactants and products.       (a) cyclohexanol +Na2Cr2O7/H2SO4, H2O -------> A        (b)  A + Et2NH/H2SO4 ----->B
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Alcohols, Ethers, and Epoxides: Crash Course Organic Chemistry #24; Author: Crash Course;https://www.youtube.com/watch?v=j04zMFwDeDU;License: Standard YouTube License, CC-BY