Would you expect but-2-ene or 2-methylbut-2-ene to react more quickly with HBr?

What is the major product of each of the following reactions, assuming that one equivalent of each reagent is used in each reaction?

c.

Predict the product(s) of each of the following reactions. If you expect a racemic mixture, draw both enantiomers.

(c)

Suggest an alkene that, upon reaction with the appropriate hydrohalic acid, will produce only the alkyl halide shown. [Ignore stereochemistry.]

(b)

What is the expected product for the reaction of each of the following alkenes with (i) HBr and (ii) HCl?

(d)

If you react carvone with a single equivalent of HBr, only one product is produced, even though carvone has two carbon–carbon double bonds. Explain this observation.

The reaction of (E)-3-chlorohex-3-ene with HCl results in the selective formation of 3,3-dichlorohexane instead of 3,4-dichlorohexane. Explain this result.

Predict the product(s) that would result when the alkenes shown here are allowed to react under the following conditions: (i) HBr;

(b)

Predict the product(s) that would result when the alkenes shown here are allowed to react under the following conditions:(ii) HCl;

(b)