C6H5 HCI C3H5 C-C¢H5 ÓH ČI This equation shows the reaction of trans-2,3-diphenyloxirane with hydrogen chloride to form 2-chloro-1,2-diphenylethanol. How many total stereoisomers are possible for 2-chloro-1,2-diphenylethanol? Given that opening of the epoxide ring in this reaction is stereoselective, provide the names of the only two isomeric products formed using IUPAC guidelines. v2-chloro-1,2-diphenylethanol product 1: (1R 2R) product 2: (1S 2S) V2-chloro-1,2-diphenylethanol

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C6H5
HCI
C3H5
C-C¢H5
ÓH ČI
This equation shows the reaction of trans-2,3-diphenyloxirane with hydrogen chloride to form 2-chloro-1,2-diphenylethanol.
How many total stereoisomers are possible for 2-chloro-1,2-diphenylethanol?
Given that opening of the epoxide ring in this reaction is stereoselective, provide the names of the only two isomeric products formed using IUPAC guidelines.
v2-chloro-1,2-diphenylethanol
product 1: (1R 2R)
product 2: (1S 2S)
V2-chloro-1,2-diphenylethanol
Transcribed Image Text:C6H5 HCI C3H5 C-C¢H5 ÓH ČI This equation shows the reaction of trans-2,3-diphenyloxirane with hydrogen chloride to form 2-chloro-1,2-diphenylethanol. How many total stereoisomers are possible for 2-chloro-1,2-diphenylethanol? Given that opening of the epoxide ring in this reaction is stereoselective, provide the names of the only two isomeric products formed using IUPAC guidelines. v2-chloro-1,2-diphenylethanol product 1: (1R 2R) product 2: (1S 2S) V2-chloro-1,2-diphenylethanol
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