Using a sample of trans-2-pentene, how could you prove that the addition of Br2 forms a cyclic bromonium ion intermediate rather than a carbocation intermediate?

What factor seems to be responsible for the Wagner-Meerwein rearrangement of camphene to give isobornyl acetate (a 3º → 2º carbocation rearrangement)?

What is the product of E2 elimination or (3R,4R)-3-chloro-2,2,4-trimethylhexane?

Based on what you know about the relative stabilities of alkyl cations and benzyliccations, predict the product of addition of HBr to 1-phenylpropene

The 3D image below is that of an allylic carbocation intermediate formed by the protonation of a conjugated diene with HBr. Draw structural formulas for the final reaction products.

What would be the major product obtained from the reaction of Br2 with 1-butene if the reaction were carried out in the solvent dichloromethane? Draw the molecule.

What would the major organic reaction product be from the reaction of 1-bromo-1-methylcyclopentane withsodium hydroxide? Would the elimination reaction outcome be affected if a student accidentally adds sodium tertbutoxide instead of sodium hydroxide?

In the Grignard Reaction experiment what would the reaction mechanism be if the reactants are Magnesium, 2-bromopropane, 4-benzaldehyde, phosphoric acid and diethyl ether, resulting in a product of 1-(4-methoxyphenyl)-2-methylpropan-1-ol

What products will be obtained mainly by nitration of 2-methylbutane? Write a reaction scheme and indicate the reaction conditions

A student was randomly given compounds E and F from the group of compounds below and asked to identify them according to their functional group. The student initially thought this to be easy, only to discover that he was embarking on some kind of Herculean task. If you were to correctly advise the student, which test will be most appropriate to distinguish compounds E and F? A. Brady's test (2,4-DNP) B. Reaction with Jones's reagent C. Tollen's test D. Iodoform test