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.
They have the same number of electrons in their outer shells. Elements in the same group often share similar chemical properties because the outer electrons generally determine a lot of their properties
2Nabr +Ca(oh)2——->CaBr2+2NaOH
Answer:
In both nuclear and chemical reactions, two physical quantities are seen to be conserved and unchanging: the number of particles and the total charge. A constant number of particles in nuclear reactions does not imply that mass is conserved.
Explanation:
