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- Draw all possible configurational stereoisomers for the given molecule below. Designate the R/S on the stereogenic centers and E/Z on the C=CWhat is the structures of A-C and what’s the stereochemistry of them.?He’s my work for c and d. I just want to know if my stereochemistry is correct. Will they have enantiomers?
- help ! a. What is the relationship between (+)-neomenthol and (-)-menthol? b. Assign absolute stereochemistry (r/s) to each of the stereocenters in (+)-menthol and (-)-menthol (DRAW) c.. Draw the structures of all of menthol's stereoisomerz .. THanks..label the stereocenters r,s,e,z and specify if any are meso. whats are the products to each orher? draw the chair conformationd and explain which one is the most stable for both products. are ha and hb homo/enantio/diasterio/hetero topic? also hc and hd.Methylcyclohexane: Axial to Equatorial Interconversion 1) How does the methyl group substituent change the conformational preferences relative to unsubstituted cyclohexane? 2) How does the methyl group substituent affect the barrier for interconversion from one chair conformation to another? Does the methyl substituent freeze the ring from interconverting or significantly slow it down?
- 1.Draw both cis- and trans-1,4-dimethylcyclohexane in their conformations. (a) How many stereoisomérs are there of cis-1,4-dimethylcyclohexane, and how many of rans-1,4-dimethylcyclohexane? (b) Are of the structures chiral? (c) What are the stereochemicar relationships among the various stereoisomers of 1,4-dimethylcyclohexane?For the following molecules: a. How many stereogenic centers are present? b. How many stereoisomers are possible for these molecules?Can someone explain which carbon the stereochemistry is inverted and how to arrive at the specific stereospecific product?