Vapour-liquid equilibrium of a two-component ideal solution of trichloroethene (C2HCl3) and trichloromethane (CHCl3) is establis
1 answer:
You might be interested in
Answer:
Pentan-2-ol
Explanation:
On this reaction, we have a <u>Grignard reagent</u> (ethylmagnesium bromide), therefore we will have the production of a <u>carbanion</u> (step 1). Then this carbanion can <u>attack the least substituted carbon</u> in the epoxide in this case carbon 1 (step 2). In this step, the epoxide is open and a negative charge is generated in the oxygen. The next step, is the <u>treatment with aqueous acid</u>, when we add acid the <u>hydronium ion</u> () would be produced, so in the reaction mechanism, we can put the hydronium ion. This ion would be <u>attacked by the negative charge</u> produced in the second step to produce the final molecule: <u>"Pentan-2-ol".</u>
See figure 1
I hope it helps!
Below Mechanism shows the mechanism of formation of diazonium ion. Aniline is treated with Nitrosonium ion which is generated in situ by the reaction of Sodium nitrile and strong acid. The resulting <span>benzenediazonium ion on reaction with CuBr yields Bromobenzene and on treatment with CuCN gives Benzonitrile. Mechanism is as folow,</span>
