Compound W, C3H17Br, and X, C3H1701, are products of the radical bromination (w), and chlorination (X), of 2,4-dimethylh

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Compound W, C3H17Br, and X, C3H1701, are products of the radical bromination (w), and chlorination (X), of 2,4-dimethylh

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Compound W C3h17br And X C3h1701 Are Products Of The Radical Bromination W And Chlorination X Of 2 4 Dimethylh 1
Compound W C3h17br And X C3h1701 Are Products Of The Radical Bromination W And Chlorination X Of 2 4 Dimethylh 1 (53.15 KiB) Viewed 14 times
Compound W, C3H17Br, and X, C3H1701, are products of the radical bromination (w), and chlorination (X), of 2,4-dimethylhexane. W and X are each chiral. W reacts readily in water to form a chiral substitution product Y, C8H170H. Reaction of a single enantiomer of W produces a single enantiomer of Y as the only substitution product. X likewise reacts readily in water though at a slower rate than W; a chiral substitution product Z, C8H170H, is again formed. Unlike w, however, reaction of a single enantiomer of X produces Z that is nearly racemic. Propose structures for W and X. • Do not use stereobonds in your answer. • In cases where there is more than one possible structure for each molecule, just give one for each. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate structures with + signs from the drop-down menu. OOO. Sn [1+ [ Previous Next
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