Organic Chemistry
Organic Chemistry
11th Edition
ISBN: 9781118133576
Author: T. W. Graham Solomons, Craig Fryhle
Publisher: Wiley, John & Sons, Incorporated
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Chapter 13, Problem 5PP

Practice Problem 13.5

The following enol (an alkene-alcohol) and keto (a keto ne) forms of C 2 H 4 O differ in the positions for their electrons, but they are not resonance structures. Explain why they are not.

Chapter 13, Problem 5PP, Practice Problem 13.5 The following enol (an <x-custom-btb-me data-me-id='56' class='microExplainerHighlight'>alkene</x-custom-btb-me>-alcohol) and keto (a keto ne) forms of C2H4O

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Sn2 (а) СН,СH-ONa + CH;CH-CI Br + NaCN SN2 (b) SN2 -S- *Na + CH3CH,Br (c) SN2 + Na*:C= (d) SN2 (e) N + Mel S2 (f) Br + excess NH3 CI SN2 + NaOH (g) (a cyclic ether) ОН SN2 (h) Br + NaOH
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
(a) Tsomane and Nyiko were given a task of synthesising methylenecyclohexane 2. After a brief discussion with each other, Tsomane proposed Method A to synthesise 2 from cyclohexanone 1 while Nyiko proposed Method B that started from hydroxymethylcyclohexane 3. Each student believed that their proposed method is better than the other. (Scheme below) (1) 1 Ph THF A Ph Ph B H₂SO4 100 °C 3 OH What is the name of the reaction that is followed by reaction Method A?

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