Organic Chemistry, Binder Ready Version
Organic Chemistry, Binder Ready Version
2nd Edition
ISBN: 9781118454312
Author: David R. Klein
Publisher: WILEY
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Chapter 3, Problem 57IP
Interpretation Introduction

Interpretation:

More acidic nature of salicylic acid than its constitutional isomers is needed to be explained.

Concept introduction:

Constitutional isomers:

  • Constitutional isomers are isomers which have the same molecular formula and different bond connectivity between the atoms in the molecule.

Acidic strength of the molecule depends on the stability of the Conjugate anion.

  • If the conjugate anion is more resonance stabilized, the acid considered as strong acid and the anion is weak base.
  • If more sterically hindered the group, acidic nature is less. That means bulkiness decreases the acidic strength of the molecule. 

To give: the explanation for the acidity of salicylic acid than para-hydroxybenzoic acid.

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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.
Question 6 What is the major product of the following Diels-Alder reaction? ? Aldy by day of A. H о B. C. D. E. OB OD Oc OE OA
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