Q2(a)(i). A para-Claisen crossover experiment
Predict the products on heating the two ortho-blocked allyl aryl ethers together. What mechanistic information follows? [structures of the two ethers given in the paper]
Answer in brief
Each ether gives its own para-rearranged phenol. The two allyl chains are not exchanged between the aromatic rings.
Part of VKC Basic
Read the key points and the full model answer with VKC Basic
VKC Basic (₹999 for 6 months) opens every solved answer, the notes, the handbook and the daily answer archive. Every Mains test series includes it.
The full model answer
As written for the answer booklet: the diagram carries the working, the lines stay short. Read here only; it is not offered as a download.
Coverspara-Claisen rearrangementcrossover experiment[3,3] sigmatropic shiftallyl aryl etherintramolecular mechanism
All parts of Question 2
- 2(a)(i) A para-Claisen crossover experiment5 marks
- 2(a)(ii) Kinetic and thermodynamic enolates5 marks
- 2(b)(i) Photolysis of an ortho-methyl diazo compound5 marks
- 2(b)(ii) Bridgehead carbocation stability5 marks
- 2(b)(iii) Rearrangement during solvolytic elimination5 marks
- 2(c)(i) Hofmann elimination10 marks
- 2(c)(ii) Chugaev elimination5 marks