ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
ORGANIC CHEM. VOL.1+2-W/WILEYPLUS
12th Edition
ISBN: 9781119304241
Author: Solomons
Publisher: WILEY C
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Chapter 9, Problem 19PP
Interpretation Introduction

Interpretation:

Thechemical formula and the structure for the given mass spectrum and 1HNMR spectrum details are to be determined.

Concept introduction:

Mass spectrometry is the detection of ions on the basis of their weights and charges and their abundance.

Mass spectroscopy is a graph with the mass (m/z) of ions on the xaxis, where m is the mass of the ion and z is the charge of the ion, and their abundance on the yaxis.

Molecular ions formed by EI mass spectrometry are high energy species. Cleavage of a single bond produces a cation and a radical. The Cation can be detected using positive ion mass spectrometry and since the radical is not charged, it will be undetected.

Chain branching or cleavage of a single bond at branch points will occur such that the carbocation formed is more stable.

Carbon-carbon bonds adjacent to atoms with unshared electron pair break readily to form carbocations which are stabilized due to resonance.

Nuclear magnetic resonance spectroscopy is a graph showing the characteristic energy absorption frequencies and intensities of a compound under a magnetic field.

Chemical shifts are the positions of signals along the x-axis in the nuclear magnetic spectroscopy. It gives an idea of how many different hydrogens are present in a given H-NMR for a particular compound.

Number of peaks=n+1, where n is the number of vicinal and geminal hydrogen atoms that are unequal to the number of hydrogen atoms producing the signal.

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Chapter 9 Solutions

ORGANIC CHEM. VOL.1+2-W/WILEYPLUS

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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