List the following compounds in order of reactivity towards MeOH (1 = highest, 4 =lowest) and propose a quantitative explanation why. 3. List the following compounds in order of reactivity towards MeOH (1 = highest, 4 =lowest) and propose a quantitative explanation why.xa xoi xoOHBrSO₂CF3

The given reactants are tertiary halide.Also the nucleophile is weak.So it follows SN1 nucleophilic…

Answered: 3. List the following compounds in…

3. List the following compounds in order of reactivity towards MeOH (1 = highest, 4 = lowest) and propose a quantitative explanation why. CI x OH SO₂CF3 x Br

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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List the following compounds in order of reactivity towards MeOH (1 = highest, 4 =
lowest) and propose a quantitative explanation why.

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4. The 1H NMR spectrum shown below corresponds to one of the molecules A-D. Identify the molecule and then provide the complete IUPAC name for the molecule. Don't forget about stereochemistry. он ÕH ÕH B D 11 10 8 6 5 1 'H NMR: 3.35 (1H, m), 1.66 (1H, m), 1.36 (9H, m, overlapping signals), 0.91 (6H, d), 0.90 (3H, t)
QUESTION 6 Propose the structure of the following alcohol? Molecular formula C5H120 The following peaks are found in proton NMR spectrum 0.91 0 (3H, triplet) 1.19 (6H, singlet) 1.50 (2H, quartet) 2. 0 (1H, singlet)
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What would be the major product of this reaction? Discuss the 1H-NMR spectrum of the product and significant changes between the starting material and your product.
1. There are several isomeric alkanes of molecular formula C6H14.Two of these exhibit the following 1H-NMR spectra. Propose a structure for each of the isomers. Isomer A: δ = 0.84 (d, 12 H), 1.39 (septet, 2H) ppm Isomer B: δ = 0.84 (t, 3 H), 0.86 (s, 9H), 1.22 (q, 2H) ppm
Reaction of (CH3)2CO with LiCCH followed by H2O gives compound X, which has a molecular ion in the mass spectrum at 84. It also has prominent absorptions in the IR spectrum at 3600-3200, 3303, 2938, and 2120 cm-1. The proton NMR shows a singlet at 1.53 (6H), a singlet at 2.37 (1H) and a singlet at 2.43 (1H). What is the structure for compound X?
Give me detailed Solution with explanation needed...don't give Handwritten answer