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- Molecular halogen (X2) adds to alkenes to make vicinal dihalides. In the boxes, draw thecurved arrow notation for the reaction.(b) Consider the reaction of 1-bromobutane with a large excess of ammonia (NH3). Draw the reactants, the transition state, andthe products. Note that the initial product is the salt of an amine (RNH3+ Br - ), which is deprotonated by the excess ammonia to give the amine.Rank the following carbocations from most stable to least stable:
- 1. When you add H-Br in a terninal alkene, the product has the rule od Markovnikov? 2. The type pf intermetary thag forms when we add HgSO4/H2SO4/H2O in an alkyl is? Please solve my both questions.thank you.Which alkene choices and reaction conditions created this product?Which of the following alkenes (a-c) reacts faster with HI?
- What other alkene is also formed along with Y in Sample Problem 9.3? What alkenes would form from X if no carbocation rearrangement occurred?plz shw the steps include alkens and alkynesWhich of the following alkene addition reactions is regioselective?A) HalogenationB) Hydration C) Both A and BD) Neither A and B
- What steps are needed to convert Y to the alkene Z ?Consider a reaction where cis-but-2-ene is treated with sO followed by NaHSO/H, O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.What alkene is the major product formed from attached alkyl halide in an E1reaction?