Organic Chemistry: Structure and Function
Organic Chemistry: Structure and Function
8th Edition
ISBN: 9781319079451
Author: K. Peter C. Vollhardt, Neil E. Schore
Publisher: W. H. Freeman
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Chapter 2, Problem 43P
Interpretation Introduction

Interpretation: Three discrete steps for acid-catalyzed hydration of alkene substrate to products for below reaction should be drawn with curved arrows.

  Organic Chemistry: Structure and Function, Chapter 2, Problem 43P

Concept introduction: The fundamental electrostatics suggests that electrons have more affinity for electron deficient sites in an organic compound. or positive charge. The curved arrow is appropriate mechanism to depict electron movement that occurs from electron rich species to electron deficient species.

Acid-catalyzed hydration is the electrophilic addition of water. The reactive species that act as a catalyst is H3O+ . In the second stage water, itself acts as a nucleophile and abstracts a proton to hydration product. The carbocation rearrangement via hydride or alkyl shift can also be found in such reactions.

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Please 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.…
I understand what the question is asking, but I'm not sure how NaNH2 and CH3CH2Br will play into the final answer. I do know that this is an alkylation of an alkyne.
Complete the table below with all the missing information. Note: more than one reactant/reagent/product may be required in a row/column.
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