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- 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.Explain why two substitution products are formed in the attached reaction.What would the molecule marked by the ? look like? How do these reagents interact with the molecules to form the product?
- For each organic reaction, say whether at equilibrium there will be more reactants than products (so equilibrium lies ro the left), or more products than reactants (so equilibrium lies to the right)...(Organic chemistry) Fill in the missi starting materials or reagentsPlease answer this Can you give examples to explain Addition reactions-general characteristics Benzene rings do not reactthi like alkenes Remember, the electrophile adds to the less substituted carbon, and the nucleophile to the more substituted carbon. Markovnikov’s Rule: The addition of a hydrogen halide to an alkene favors the product in which the proton adds to the alkene carbon that is initially bonded to the greater number of hydrogen atoms. Carbocation rearrangements- Methyl groups and hydride groups can migrate to make a more stable carbocation. A primary carbocation is less stable than a secondary carbocation, which is less stable than a tertiary carbocation. Addition of A Strong Bronsted Acid Hydrohalogenation HX addition to an alkene. Goes through a carbocation intermediate. The electrophile (H+) adds to the less substituted carbon, and the carbocation forms on the more substituted carbon. The nucleophile (X-) then adds to the more substituted carbocation.…
- TOPIC: Preparation of Ethylene Expound and explain the given answer to the question.I don't understand where the H goes for the first product. I'm not sure exactly what the question is asking for. Would this be considered a substitution reaction even though there are two products?PLEASE COMPLETE THE REACTION. IT IS LIKE THIS IN BOOK.
- 2. Draw one enol tautomer of each of the following ketones and aldehydes. a) b) c) of مل G H1. Addition of HBr to alkenes occurs according to rule. Your answerDraw what would happen to 2,5-dimethyl-2-hexene in an alkyl halides and alkane reaction. This is for a concept map. So what would the alkene 2,5-dimethyl-2-hexene be as an alkyl halides and how to you go from an alkene to an alkane with 2,5-dimethyl-2-hexene. No bond lines. I know this much for alkene to alkane