Enantiomerically pure (R)-(+)-2-methyl-1,2-butanediol has a specific rotation [] 20 D + 19.3 degrees mL g 1 dm
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Enantiomerically pure (R)-(+)-2-methyl-1,2-butanediol has a specific rotation [α]20D + 19.3 degrees mL g–1 dm–1 in chloroform solution.
(a) What is the EE of a mixture of (+)- and (-)-2-methyl-1,2-butanediol that has an apparent specific rotation of 26.3 degrees mL g–1 dm–1 under the same conditions?
(b) What percentage of each enantiomer is present in the mixture?
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