**Question 2:**Going from left to right, classify each halide as 1°, 2°, or 3°. Determine which substitution mechanism will most likely occur with the substrates shown below:**Structures:**1. **Structure 1**: A chlorine (Cl) atom is attached to a primary carbon, which is connected to a linear alkyl chain.2. **Structure 2**: A chlorine (Cl) atom is attached to a secondary carbon in a branched alkyl chain.3. **Structure 3**: A chlorine (Cl) atom is attached to a tertiary carbon in a highly branched alkyl chain.4. **Structure 4**: A chlorine (Cl) atom is attached to a benzene ring, making it an aryl halide.5. **Structure 5**: A chlorine (Cl) atom is attached to a primary carbon in a simple linear chain.6. **Structure 6**: A chlorine (Cl) atom is attached to a tertiary carbon in a branched alkyl chain.For each structure, determine if the substitution mechanism is likely to be SN1 or SN2, considering the degree of the carbon where the chlorine is attached.

Halide anion attached with carbon classify the alkyl halide as 1◦, 2◦, 3◦.

Answered: 2. Going from left to right, classify…

2. Going from left to right, classify each halide as 1°, 2° or 3°. Determine which substitution mechanism will most likely occur with the substrates shown below: CI to CI CI CI

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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1. Name the major product or describe it 2. Draw the product
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lost on this guy as well Be sure to answer all parts. Determine a stepwise mechanism for the following reaction that illustrates why two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a wide ph Meme under Sx1 reaction conditions, even though it is a 1° alkyl halide. 1-bromohex-2-ene CH₂OH Part 1: The first step in the reaction proceeds according to which mechanism? CH₂CH₂CH₂CH=CHCH₂ CH₂CH₂CH₂CH=CHCH₂ + CH₂OH Part 2 out of 5 Draw the missing resonance contributor. Check my work OCH₁ CH₂CH₂CH₂CH=CH-CH₂ + Br CH₂CH₂CH₂CH=CHCH₂ CH OCH₂ edit structure... Next part +HBr
4
could you propose a mechanism?
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