Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
Answer:
74.344 kJ.
Explanation:
Below is an attachment containing the solution.
<u>Answer:</u> The product side must be 
<u>Explanation:</u>
Single displacement reaction is defined as the reaction in which more reactive metal displaces a less reactive metal from its chemical reaction.

Metal C is more reactive than metal A.
The reactivity of metal is determined by a series known as reactivity series. The metals lying above in the series are more reactive than the metals which lie below in the series.
Law of conservation of mass states that mass can neither be created nor be destroyed but it can only be transformed from one form to another form. This also means that total number of individual atoms on reactant side must be equal to the total number of individual atoms on the product side.
When zinc metal reacts with hydrochloric acid, it leads to the production of zinc chloride and hydrogen gas. The chemical reaction follows:

<u>On reactant side:</u>
Number of zinc atoms = 1
Number of hydrogen atoms = 2
Number of chlorine atoms = 2
<u>On product side:</u>
Number of zinc atoms = 1
Number of hydrogen atoms = 2
Number of chlorine atoms = 2
Hence, the product side must be 