Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter SRP, Problem 23P

What are compounds A and B? Compound B has a strong IR absorption band in the 1650–1730 cm 1 region and a broad strong band in the 3200–3550 cm 1 region.

1-Methylcyclohexene (2) NaHSO 3  (1) OSO4  A ( C 7 H 14 O 2 ) CH 3 CO 2 H  CrO 3   ( C 7 H 12 O 2 )

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Compound X (structure shown below) has a molecular formula C5H1o and reacts with H2/Pt to give compound Y, C5H12. What is the name of the reaction involved to produce Compound Y? H2C H3C CH3 Hydration Hydrogenation Halogenation Addition of halohydrin
A compound (C7H14O) has a strong peak in its IR spectrum at 1710 cm–1. Its 1H NMR spectrum consists of three singlets in the ratio 9:3:2 at δ 1.0, 2.1, and 2.3, respectively. Identify the compound.
A compound has the molecular formula C5H1002. Its IR spectrum shows a strong absorption band near 1740 cm1. Its 'H NMR spectrum consists of two singlets at Õ 1.2 and o 3.6. Which is the most likely structure of the compound?

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NMR Spectroscopy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=SBir5wUS3Bo;License: Standard YouTube License, CC-BY