Organic Chemistry: Principles And Mechanisms
Organic Chemistry: Principles And Mechanisms
2nd Edition
ISBN: 9780393663549
Author: KARTY, Joel
Publisher: W. W. Norton and Company
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Chapter 11, Problem 11.29P
Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the addition of HCl to dihydropyran is to be drawn, and the major product is to be predicted.

Concept introduction:

The electrophilic addition of H+ to the C=C double bond produces carbocation intermediate. The more stable carbocation proceeds to the next coordination step. In the next step, the nucleophile attacks the positively charged C+ carbon atom to form a neutral product.

The carbocation intermediate is a trigonal planar, and the nucleophile can attack the C+ from the front (wedge) or from behind (dash). This leads to two different products.

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Students have asked these similar questions
Use diagram to answer the following:  1.Is the overall rxn endo- or exothermic. Explain briefly your answer____________________2. How many steps in this mechanism?_____________3. Which is the rate determining step? Explain briefly your answer____________________4. Identify (circle and label) the reactants,the products and intermediate (Is a Cation, Anion, or a Radical?) Please explain and provide full understanding.
Draw the entire mechanism and add Curved Arrows to show clearly how electrons areredistributed in the process.   Please explain and provide steps clearly.
15) Create Lewis structure Br Br

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Organic Chemistry: Principles And Mechanisms

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