Organic Chemistry - Standalone book
Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
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Chapter 19.15, Problem 10P
Interpretation Introduction

Interpretation:

The structure of the hydroxyl acid corresponding to the given lactones are to be written.

Concept Introduction:

Retrosynthesis is used to identify the reactants. It involves the breaking of the target molecule into starting materials.

Carboxylic acids react with alcohols in the presence of acid as a catalyst to form esters as the product. This reaction is known as Fischer esterification. The intramolecular esterification of γ, and δ-hydroxy carboxylic acids lead to the formation of five- and six-membered lactones respectively.

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7) 8) FCI II -C-C-C=C-C || Br Br || -C=C-Br -CEC-C-C- 10) 11) F Br i OH مله 12) Br i 13) 14) 15) CH3CHFCHFC=CH C(OH)Br2CHF(CH2)4CH2CH3 CH3(CH2)3CH=CH(CH2)2CH3
Name 1) 3-fluoro, 1-butene 2) 2-heptene 2,3-difluoro- 1-pentene 4) 6-iodo,4-methyl- 2-decyne 5) 4,4-dibromo- 1,2-butandiol Complete structural formula F -C=C-C-C- Line formula Condensed structural formula N F CH2=CHCHFCH3
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