The following equation shows the reaction of trans-2,3-diphenyloxirane with hydrogen chloride in benzene to form 2-chloro-1,2-diphenylethanol. H CH; CH, + HCI C,H;CH-CHC,H, НО ČI trans-2,3-Diphenyloxirane 2-Chloro-1,2-diphenylethanol

The following equation shows the reaction of trans-2,3-diphenyloxirane with hydrogen chloride in benzene to form 2-chloro-1,2-diphenylethanol. H CH; CH, + HCI C,H;CH-CHC,H, НО ČI trans-2,3-Diphenyloxirane 2-Chloro-1,2-diphenylethanol

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter16: Chemistry Of Benzene: Electrophilic Aromatic Substitution

Section16.3: Alkylation And Acylation Of Aromatic Rings: The Friedel–crafts Reaction

Problem 6P: What is the major monosubstitution product from the Friedelâ€”Crafts reaction of benzene with 1...

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Concept explainers

Stereochemistry and Isomerism

Stereochemistry deals with the three-dimensional structure and properties of molecules. It explains the arrangement of atoms and their manipulation within a molecule in a 3D structure. Stereochemistry can be dealt with all types of molecules. Based on the stereochemistry of a molecule, the physical and chemical properties of the molecules vary.

Question

How many stereoisomers are possible for 2-chloro-1,2-diphenylethanol?

The following equation shows the reaction of trans-2,3-diphenyloxirane with hydrogen
chloride in benzene to form 2-chloro-1,2-diphenylethanol.
H
CH;
CH,
+ HCI
C,H;CH-CHC,H,
НО
ČI
trans-2,3-Diphenyloxirane
2-Chloro-1,2-diphenylethanol

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