Get Ready for Organic Chemistry
Get Ready for Organic Chemistry
2nd Edition
ISBN: 9780321774125
Author: KARTY, Joel
Publisher: PEARSON
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Chapter G, Problem G.3P
Interpretation Introduction

Interpretation:

A peak appears at m/z = 83 in the mass spectrum of hept-3-ene. The fragmentation of hept-3-ene’s molecular ion produces the ion that gives rise to this peak is to be shown. The reason we think the peak at m/z = 83 is smaller than the one at m/z = 69 is to be explained.

Concept introduction:

The mass of hept-3-ene is 98 u. The π- electron of the C-C bond is ejected in the ionization process to produce the molecular ion. Hept-3-ene is not symmetrical, and there are two allylic C-C bonds, so fragmentation can happen via two routes.

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Choose the Lewis structure for the compound below: H2CCHOCH2CH(CH3)2 HH H :d H H H C. Η H H HH H H H H. H H H HH H H H H H- H H H C-H H H HHHH
Each of the highlighted carbon atoms is connected to hydrogen atoms.
く Complete the reaction in the drawing area below by adding the major products to the right-hand side. If there won't be any products, because nothing will happen under these reaction conditions, check the box under the drawing area instead. Note: if the products contain one or more pairs of enantiomers, don't worry about drawing each enantiomer with dash and wedge bonds. Just draw one molecule to represent each pair of enantiomers, using line bonds at the chiral center. More... No reaction. Explanation Check O + G 1. Na O Me Click and drag to start drawing a structure. 2. H + 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility 000 Ar P
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