I just answered your other question and wrote all the definitions of the terms. I would say this is probably refering to Fusion because you are fusing together more nuclei into one nucleus. Fusion= bringing separate things into one entity.
I think its becuse the shoreline is shalow water that is warmed by the sun? ...... I may be rong
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.
The right answer for the question that is being asked and shown above is that: "C) carbon monoxide and carbon dioxide" hydrocarbons burn completely in an excess of oxygen, the products are <span>C) carbon monoxide and carbon dioxide</span>
