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Please help answer the attached question..thank you!
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- (a) Draw all stereoisomers formed by monochlorination of the cis and trans isomers of 1,2-dimethylcyclobutane drawn below. (b) How many constitutional isomers are formed in each reaction? (c) Label any pairs of enantiomers formed.a) What are the differences between major and minor stereoisomers. b) how can we use major and minor products to determine stereospecificity in an experiment.How much of the R enantiomer is present in 10g of a mixture that has an enantiomeric excess of 30% of the S isomer?