Organic Chemistry
Organic Chemistry
3rd Edition
ISBN: 9781119338352
Author: Klein
Publisher: WILEY
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Chapter 17.5, Problem 15ATS
Interpretation Introduction

Interpretation For the given compounds, it should be determined which compound is expected to have lower pKa value

Concept introduction:

  • Ka is the acid dissociation constant of a solution
  • pKa=-log10[Ka]
  • For the stronger acids pKa value will be lower and  more stable
  • For the weaker acids pKa value will be higher and less stable
  • For stronger acids, its conjugate base is more stable
  • For weaker acids, its conjugate base is less stable.
  • Conjugate base is formed by the deprotonation of the parent acid
  • Aromatic compounds are more stable than non-aromatic compound
  • In order for the heterocycle to achieve a continuous system of overlapping p orbitals, the lone pair of the hetero atom must occupy a p orbital with six π electrons that is four from the π bonds and two from the lone pair. Then this compound is aromatic.

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option choice:  Isoleucine Histidine Threonine Alanine Lysine Aspartate Tryptophan Tyrosine Leucine Arginine Cysteine Asparagine Valine Glutamine Glycine Methionine Serine Proline Phenylalanine Glutamate
sketch the nature of the metal-alkylidene bonding interactions.
Part C The perspective formula of isoleucine, an amino acid, is provided below. HOOC H₂NIC H 川 CH3 CH,CH3 Draw the Newman projection in staggered conformation for isoleucine by viewing the molecule along the C-2-C-3 bond. 1. Edit the Newman projection on the canvas. 2. Replace the appropriate hydrogens with the appropriate -CH3 or other groups. 3. If you need to start over, Undo or choose a Newman projection from the Templates toolbar (bottom). Important: Never delete the hydrogen atoms or bonds directly attached to the template, and do not move them by dragging or dropping them. That will break the projections structures. Only replace them! ▸ View Available Hint(s) 0 2 H± 3D EXP. L ד י CONT. 2 H 0 N о

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Organic Chemistry

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