Predict the alkyne and reactants you might use to make the following haloalkenes. [Providing the reactant and the reagent is how we start thinking about synthesis.]
(b)

For the alkynes shows here, show the product(s) expected to form when treated under the following conditions: (v) HCl (2 equiv.). If you expect two products, show both.

(c)

Predict the alkyne and reactants you might use to make the following haloalkenes. [Providing the reactant and the reagent is how we start thinking about synthesis.]

(a)

HBr and peroxides are also used to generate 1-bromo-1-alkenes. Suggest a starting reactant that would successfully undergo this reaction.

Predict the major products resulting from the addition of one equivalent of HX to the following alkynes.

(b)

The addition of H―X to alkynes has been shown to occur predominately via anti addition:

Two chemists disagreed on whether or not anti addition would happen on terminal alkynes as well. Suggest an experiment through which you could resolve this dispute.

What is the major product obtained from the reaction of each of the following compounds with excess HCl?

c. CH₃CH₂C☰CCH₂CH₂CH₃

Answer Problem 39, parts a–h, using 2-butyne as the starting material instead of propyne.

a. HBr (1 mol)

b. HBr (2 mol)

Predict the major product(s) of the following reactions:

c. cyclooctyne + 2 HBr

d. *hex-2-yne + 2 HCl