Organic Chemistry 3rd.ed. Klein Evaluation/desk Copy
Organic Chemistry 3rd.ed. Klein Evaluation/desk Copy
3rd Edition
ISBN: 9781119320524
Author: Klein
Publisher: WILEY
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Chapter 14, Problem 67IP
Interpretation Introduction

Interpretation: The relative heights for the peaks at M,M+2andM+4 for the given compound should be predicted under given conditions.

Concept Introduction:

Mass spectroscopy: It is a form of spectroscopic technique which is used for the elucidation of the molecular formula and molecular weight of the compound, depending upon the mass of the molecule.

Molecular formula: It represents the types of atoms with their total number present in a given molecule.

Molecular ion peak (M)+· : It is defined as the heaviest peak in the IR spectrum of the molecule which represents the largest molecular ion in the given molecule with greater m/z value.

Base peak: It is the tallest peak in the spectrum.

The (M+1)+· peak: It denotes the peak that arises next to molecular ion peak in the mass spectrum. The peak arises due to the presence of the isotope of carbon since carbon has one isotope (13C).

The (M+1)+· peak in mass spectroscopy is used to explain the number of carbon atoms present in a molecule depending on the abundance of (M+1)+· peak.

The (M+2)+· peak: It denotes the peak that arises next to molecular ion peak in the mass spectrum with respect to the presence of major isotopes in the molecule especially it is used to find the presence of chlorine and bromine since they has two isotopes.

The Hydrogen Deficiency Index (HDI): It is used to measure the number of degrees of unsaturation (double and triple bonds) present in a given molecule. It is determined by using the formula

HDI=12[(2×No. of Carbon atoms)+2+(No. of Nitrogen atoms)-(No. of Hydrogen atoms)-(No. of halogens)]

Isotopes: The elements with same atomic number but with different mass number are said to be isotopes of each other.

To determine: The relative height for the peaks at (M)+· , (M+2)+· and (M+4)+· in given compound CH2BrCl .

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Provide the unknown for the given data.
Electron Arrangement A. Fill in the following chart relating to levels, sublevels and orbitals. Levels (n) 1 Sublevels # of Orbitals per sublevel 2 3 4 # of Electrons per sublevel Total Electrons per level Complete: B. Answer the following questions related to levels, sublevels, orbitals and electrons. 1. How many sublevels are in energy level 2? 2. How many orbitals are in a 4f sublevel? 3. How many electrons can level 3 hold? 4. How many orbitals are in level 4? 5. How many electrons can sublevel 2p hold? 11
Provide the unknown for the given details.

Chapter 14 Solutions

Organic Chemistry 3rd.ed. Klein Evaluation/desk Copy

Ch. 14.5 - Prob. 11CCCh. 14.6 - Prob. 1LTSCh. 14.6 - Prob. 12PTSCh. 14.6 - Prob. 13ATSCh. 14.7 - Prob. 2LTSCh. 14.7 - Prob. 14PTSCh. 14.7 - Prob. 15ATSCh. 14.7 - Prob. 16ATSCh. 14.7 - Prob. 17ATSCh. 14.9 - Prob. 18CCCh. 14.9 - Prob. 19CCCh. 14.10 - Prob. 3LTSCh. 14.10 - Prob. 20PTSCh. 14.10 - Prob. 21ATSCh. 14.11 - Prob. 22CCCh. 14.11 - Prob. 23CCCh. 14.12 - Prob. 24CCCh. 14.12 - Prob. 25CCCh. 14.12 - Prob. 26CCCh. 14.12 - Prob. 27CCCh. 14.13 - Prob. 28CCCh. 14.13 - Prob. 29CCCh. 14.16 - Prob. 4LTSCh. 14.16 - Prob. 30PTSCh. 14.16 - Prob. 31PTSCh. 14.16 - Strigol is an important plant hormone that is...Ch. 14 - Prob. 33PPCh. 14 - Prob. 34PPCh. 14 - Prob. 35PPCh. 14 - Prob. 36PPCh. 14 - Prob. 37PPCh. 14 - Prob. 38PPCh. 14 - Prob. 39PPCh. 14 - Prob. 40PPCh. 14 - Prob. 41PPCh. 14 - Prob. 42PPCh. 14 - Prob. 43PPCh. 14 - The mass spectrum of 2-bromopentane shows many...Ch. 14 - Prob. 45PPCh. 14 - Prob. 46PPCh. 14 - Prob. 47PPCh. 14 - Prob. 48PPCh. 14 - Prob. 49PPCh. 14 - Prob. 50PPCh. 14 - Prob. 51PPCh. 14 - Prob. 52PPCh. 14 - Prob. 53PPCh. 14 - Prob. 54PPCh. 14 - Prob. 55PPCh. 14 - Prob. 56PPCh. 14 - Prob. 57IPCh. 14 - Prob. 58IPCh. 14 - Prob. 59IPCh. 14 - Prob. 60IPCh. 14 - Prob. 61IPCh. 14 - Prob. 62IPCh. 14 - Prob. 63IPCh. 14 - Prob. 64IPCh. 14 - Prob. 65IPCh. 14 - Prob. 66IPCh. 14 - Prob. 67IPCh. 14 - Prob. 68IPCh. 14 - Compound A exists in equilibrium with its...Ch. 14 - The following two isomers were each subjected to...Ch. 14 - Myosmine can be isolated from tobacco, along with...Ch. 14 - Prob. 72IPCh. 14 - Prob. 73IPCh. 14 - Prob. 74IPCh. 14 - Prob. 75IPCh. 14 - Prob. 76CPCh. 14 - Prob. 77CPCh. 14 - Prob. 78CPCh. 14 - Prob. 79CP
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