ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
12th Edition
ISBN: 9781119664635
Author: Solomons
Publisher: WILEY
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Chapter 9, Problem 22P
Interpretation Introduction

Interpretation:

The structure for an alcohol with molecular formula C5H12O having given 1H NMR spectrum is to be proposed and chemical shifts and splitting pattern are to be specified.

Concept introduction:

Few elements such as 13C and 1H have nuclei behaving as magnets about an axis. When placed in magnetic field irradiated with electromagnetic energy of specific frequency, the nuclei tend to absorb energy via magnetic resonance. NMR spectrum is a graph between intensities of NMR peaks versus magnetic field (frequency). An NMR spectrum is used to predict the structure of molecules.

There are four features of NMR spectra that help in predicting the structure:

The number of signals in the spectra tells us the number of different types of protons present in the molecule.

Chemical shift is the measurement on δ scale (in ppm) where the peaks occur when the nuclei absorb energy through magnetic resonance. This chemical shift position of a set of protons tells us the magnetic environment around those protons, which depends upon electron density around them.

Area under the peaks tells us the number of similar protons.

The splitting pattern of a signal tells us about the number of protons present on adjacent carbon.

NMR signal of a particular proton generally splits into + 1 peaks, where N is the number of hydrogen atoms on the adjacent atoms. If there is no hydrogen present on the adjacent atom, then resonance will be singlet. If there is only one hydrogen present on adjacent carbon, then signal will split into two peaks or have doublets. Two hydrogens on adjacent atoms split the signal into three peaks, a triplet, and so on.

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Chapter 9 Solutions

ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT

Ch. 9 - PRACTICE PROBLEM 9.11 Draw the most stable chair...Ch. 9 - Prob. 12PPCh. 9 - PRACTICE PROBLEM 9.13 How many signals would you...Ch. 9 - Prob. 14PPCh. 9 - Prob. 15PPCh. 9 - Prob. 16PPCh. 9 - Prob. 17PPCh. 9 - PRACTICE PROBLEM 9.18 What are the expected ratios...Ch. 9 - Prob. 19PPCh. 9 - How many 1H NMR signals (not peaks) would you...Ch. 9 - How many 13C NMR signals would you predict for...Ch. 9 - Prob. 22PCh. 9 - Prob. 23PCh. 9 - Prob. 24PCh. 9 - Compound Q has the molecular formula C7H8. The...Ch. 9 - 9.26 Explain in detail how you would distinguish...Ch. 9 - Compound S (C8H16) reacts with one mole of bromine...Ch. 9 - A compound with molecular formula C4H8O has a...Ch. 9 - In the mass spectrum of 2, 6-dimethyl-4-heptanol...Ch. 9 - Prob. 30PCh. 9 - What are the masses and structures of the ions...Ch. 9 - Prob. 32PCh. 9 - Ethyl bromide and methoxybenzene (shown below)...Ch. 9 - 9.34 The homologous series of primary amines, ,...Ch. 9 - Propose a structure that is consistent with each...Ch. 9 - 9.36 Propose structures for compounds E and F....Ch. 9 - 9.37 Use the NMR and IR data below to propose a...Ch. 9 - 9.38 When dissolved in , a compound (K) with the...Ch. 9 - Compound T (C5H8O) has a strong IR absorption band...Ch. 9 - Prob. 40PCh. 9 - Deduce the structure of the compound that gives...Ch. 9 - Deduce the structure of the compound that gives...Ch. 9 - The 1H NMR spectrum of a solution of 1,...Ch. 9 - Acetic acid has a mass spectrum showing a...Ch. 9 - The 1H NMR peak for the hydroxyl proton of...Ch. 9 - The 1H NMR study of DMF (N, N-dimethylformamide)...Ch. 9 - 9.48 The mass spectra of many benzene derivatives...Ch. 9 - Prob. 49PCh. 9 - 1. Given the following information, elucidate the...Ch. 9 - Two compounds with the molecular formula C5H10O...
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