Answer:
1) C2H4(OH)2
Explanation:
A 1,2-ethanediol has an ethane structure consisting of two Carbon atoms with a hydrogen from each carbon substituted by a hydroxyl group. This makes it a 1,2-diol.
Answer: Thomson
Explanation: It verified J. J. Thomson's work on the atomic structure.
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:
B.
Explanation:
One mole is the amount of substance that contain the Avogadro number which is equal to 6.022×10^23 atom, molecules or ions.
Answer: Fluorine
Explanation: It belongs in the same group as Bromine
