Answer:
I didn't understand questions properly. Sorry
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.
1)water has a great capacity to hold a moderate heat energy
Answer:
The covalent bond in Cl₂ is break and combine with sodium to form NaCl through ionic bond.
Explanation:
Chemical equation:
Na + Cl₂ → NaCl
Balanced chemical equation:
2Na + Cl₂ → 2NaCl
The given reaction indicate the formation of sodium chloride.
Sodium chloride is an ionic compound. It is formed by the reaction of chlorine and sodium. The type of bond in Cl₂ is covalent. Both chlorine atoms are tightly held together through sharing of electrons. When sodium chloride is formed the covalent between the chlorine atoms are break and it react with sodium . The chlorine toms thus gain the one electron from the sodium atom and became negative ion while sodium by losing its one valance electrons became positive ions. The strong electrostatic forces are develop between them and ionic bond is formed.