EBK GENERAL CHEMISTRY: THE ESSENTIAL CO
EBK GENERAL CHEMISTRY: THE ESSENTIAL CO
7th Edition
ISBN: 9780100257047
Author: Chang
Publisher: YUZU
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Chapter 11.2, Problem 2PE
Interpretation Introduction

Interpretation:

IUPAC name of the given structure of compound has to be given.

Concept introduction:

IUPAC Nomenclature:

  • The longest continuous chain of carbon atoms is identified.
  • The substituent groups attached to the parent chain is identified. A substituent group contains group of atoms attached to the carbon atom of the chain.
  • While numbering the longest chain, the substituent should get least possible number.
  • Write the name of the compound; the parent name written as last part of the name. The name of the substituents is written as prefix and a hypen separates the number that the substituents attached with carbon. More than one substituent should be written in alphabetical order.

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What spectral features allow you to differentiate the product from the starting material? Use four separate paragraphs for each set of comparisons. You should have one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of functional group changes.

Chapter 11 Solutions

EBK GENERAL CHEMISTRY: THE ESSENTIAL CO

Ch. 11 - Prob. 11.2QPCh. 11 - Prob. 11.3QPCh. 11 - 11.4 What are structural isomers? Ch. 11 - Prob. 11.5QPCh. 11 - 11.6 Draw skeletal structures of the boat and...Ch. 11 - 11.7 Alkenes exhibit geometric isomerism because...Ch. 11 - 11.8 Why is it that alkanes and alkynes, unlike...Ch. 11 - Prob. 11.9QPCh. 11 - 11.10 Describe reactions that are characteristic...Ch. 11 - Prob. 11.11QPCh. 11 - Prob. 11.12QPCh. 11 - Prob. 11.13QPCh. 11 - Prob. 11.14QPCh. 11 - Prob. 11.15QPCh. 11 - Prob. 11.16QPCh. 11 - Prob. 11.17QPCh. 11 - 11.18 Draw Newman projections of four different...Ch. 11 - 11.19 Draw the structures of cis-2-butene and...Ch. 11 - 11.20 Would you expect cyclobutadiene to be a...Ch. 11 - Prob. 11.21QPCh. 11 - Prob. 11.22QPCh. 11 - 11.23 Sulfuric acid (H2SO4) adds to the double...Ch. 11 - Prob. 11.24QPCh. 11 - Prob. 11.25QPCh. 11 - Prob. 11.26QPCh. 11 - Prob. 11.27QPCh. 11 - Prob. 11.28QPCh. 11 - Prob. 11.29QPCh. 11 - 11.30 Benzene and cyclohexane both contain...Ch. 11 - Prob. 11.31QPCh. 11 - Prob. 11.32QPCh. 11 - Prob. 11.33QPCh. 11 - Prob. 11.34QPCh. 11 - Prob. 11.35QPCh. 11 - Prob. 11.36QPCh. 11 - Prob. 11.37QPCh. 11 - Prob. 11.38QPCh. 11 - Prob. 11.39QPCh. 11 - Prob. 11.40QPCh. 11 - Prob. 11.41QPCh. 11 - Prob. 11.42QPCh. 11 - Prob. 11.43QPCh. 11 - Prob. 11.44QPCh. 11 - Prob. 11.45QPCh. 11 - Prob. 11.46QPCh. 11 - Prob. 11.47QPCh. 11 - Prob. 11.48QPCh. 11 - Prob. 11.49QPCh. 11 - Prob. 11.50QPCh. 11 - Prob. 11.51QPCh. 11 - Prob. 11.52QPCh. 11 - Prob. 11.53QPCh. 11 - Prob. 11.54QPCh. 11 - Prob. 11.55QPCh. 11 - Prob. 11.56QPCh. 11 - Prob. 11.57QPCh. 11 - Prob. 11.58QPCh. 11 - Prob. 11.59QPCh. 11 - Prob. 11.60QPCh. 11 - Prob. 11.61QPCh. 11 - Prob. 11.62QPCh. 11 - Prob. 11.63QPCh. 11 - Prob. 11.64QPCh. 11 - Prob. 11.65QPCh. 11 - Prob. 11.66QPCh. 11 - Prob. 11.67QPCh. 11 - Prob. 11.68QPCh. 11 - Prob. 11.69QPCh. 11 - Prob. 11.70QPCh. 11 - Prob. 11.71QPCh. 11 - Prob. 11.72QPCh. 11 - 11.73 Octane number is assigned to gasoline to...Ch. 11 - Prob. 11.74SPCh. 11 - Prob. 11.75SPCh. 11 - Prob. 11.76SPCh. 11 - Prob. 11.77SPCh. 11 - Prob. 11.78SP
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