I am sure, the answer is variant B.
Be kind yk? tell him have some respect for your relationship and if he can't then cut him off completely
3NF3 + 5H2O → HNO3 + 2NO + 9HF
Nitrogen fluoride reacts with water to produce nitric acid, nitric oxide, and hydrogen fluoride. The reaction slowly takes place in a boiling solution.
CH2CH2 + H2O → CH3CH2OH
Ethylene is a hydrocarbon with water that creates ethanol and ethanol is an alcohol
This reaction is most likely to fall under SN2 because the
thing called carbonication does not occur in SN1. The carbon forms a partial
bond with the nucleophile during the intermediate phase and the leaving group.
So for this question the reaction will fall under SN2.
Carbonyl Compounds containing
alpha proton readily donates alpha acidic proton when treated with
strong Base. In given statement <span>
2-phenylacetaldehyde is converted into Enolate and Enolates acts as a nucleophile and attacks carbonyl group of
Benzaldehyde. The mechanism of given reaction is as follow, the movement of electrons is shown by
RED arrows,</span>
