In the acid-catalyzed dehydration of 2-methyl-1-propanol, what carbocation would be formed if a hydride shift accompanied cleavage of the carbon–oxygen bond in the alkyloxonium ion? What ion would be formed as a result of a methyl shift? Which pathway do you think will predominate, a hydride shift or a methyl shift?
Answer to relevant QuestionsEach of the following carbocations has the potential to rearrange to a more stable one. Write the structure of the rearranged carbocation. (a) CH3CH2CH2+ (b) (CH3)2CHC_HCH3 (c) (CH3)3CCHCH3 (d) (CH3CH2)3CCH2+Compound A (C6H14) gives three different monochlorides on photochemical chlorination. One of these monochlorides is inert to E2 elimination. The other two monochlorides yield the same alkene B (C6H12) on being heated with ...What are “oligos?”Essay Text: The history of billiards begins in the fourteenth century. The game was invented in Europe, but there was a conflict as to what country. The French believed that the English invented the game, but at the ...Essay Text: Basketball is a great game that is one of the most popular in America. In this sport you have to have good aim to shoot, good jumping skills to rebound, you have to be quick, and also have good ball ...
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