Predict the major product(s) of the following reactions:
c. cyclooctyne + 2 HBr
d. *hex-2-yne + 2 HCl

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)

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)

Show how hex-1-yne might be converted to

f. 2,2-dibromohexane.

Using hex-1-ene as your starting material, show how you would synthesize the following compounds. (Once you have shown how to synthesize a compound, you may use it as the starting material in any later parts of this problem.)

a. 1,2-dibromohexane

b. hex-1-yne

c. 2,2-dibromohexane

Predict the products of reaction of pent-1-yne with the following reagents.

a. 1 equivalent of HCl

b. 2 equivalents of HCl

c. excess H₂, Ni

Which of the following best represents the major organic product formed when a terminal alkyne reacts with one equivalent of $H_{\mathrm{Cl}}$ under standard conditions?