Organic Chemistry, Books a la Carte Edition (8th Edition)
8th Edition
ISBN: 9780134074580
Author: Bruice, Paula Yurkanis
Publisher: PEARSON
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Chapter 22.7, Problem 10P
Interpretation Introduction
Interpretation: The products, including the configuration in the given reaction has to be determined.
Concept introduction:
- Catalyst: Substance which helps in increasing the rate of a particular reaction without getting consumed in the reaction.
- Intramolecular catalysis: A catalysis where catalyst is a part of the molecule that undergoes the reaction promotes the reaction in a species.
- Intramolecular nucleophilic catalysis: A catalysis where catalyst is a part of the molecule that undergoes the reaction promotes the reaction in a species by acting as a nucleophile.
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The acid-base indicator HX undergoes the following reaction in a dilute aqueous solution:
HX (color 1) H+ + X- (color 2).
The following absorbance data were obtained for a 0.00035 M solution of HX in 0.1 M NaOH
and 0.1 M HCI. Measurements were made at wavelengths of 450 nm and 620 nm using a 1.0
cm glass cuvette.
450
620
A(460 nm) A(630 nm)
0.1 M NaOH
0.1 M HCI
0.065
0.435
0.895
0.150
In the 0.1M NaOH solution, the indicator will be almost 100% in the X- form, while in 0.1M HCI,
the indicator will be nearly 100% protonated (HX). Calculate the acid dissociation constant for
the indicator if a pH=5 buffer solution containing a very small amount of indicator exhibits an
absorbance of 0.567 at 450 nm and 0.395 at 620 nm (measured in a 1 cm glass cuvette).
Chapter 22 Solutions
Organic Chemistry, Books a la Carte Edition (8th Edition)
Ch. 22.2 - Compare each of the mechanisms listed here with...Ch. 22.2 - Prob. 3PCh. 22.2 - Prob. 4PCh. 22.3 - a. Draw the mechanism for the following reaction...Ch. 22.5 - Prob. 7PCh. 22.5 - Propose a mechanism for the Co2+ catalyzed...Ch. 22.6 - Prob. 9PCh. 22.7 - Prob. 10PCh. 22.7 - Prob. 12PCh. 22.7 - Prob. 13P
Ch. 22.9 - Which of the following amino acid side chains can...Ch. 22.9 - Which of the following C-terminal peptide bonds is...Ch. 22.9 - Carboxypeptidase A has esterase activity as well...Ch. 22.10 - Arginine and lysine side chains fit into trypsins...Ch. 22.10 - Explain why serine proteases do not catalyze...Ch. 22.11 - If H2 18O is used in the hydrolysis reaction...Ch. 22.11 - Draw the pH-activity profile for an enzyme that...Ch. 22.12 - The pHactivity profile for glucose-6-phosphate...Ch. 22.12 - Prob. 23PCh. 22.13 - Draw the mechanism for the hydroxide ion-catalyzed...Ch. 22.13 - What advantage does the enzyme gain by forming an...Ch. 22.13 - Prob. 26PCh. 22.13 - Prob. 27PCh. 22.13 - Aldolase shows no activity if it is incubated with...Ch. 22 - Which of the following parameters would be...Ch. 22 - Prob. 29PCh. 22 - Prob. 30PCh. 22 - Prob. 31PCh. 22 - Indicate the type of catalysis that is occurring...Ch. 22 - The deuterium kinetic isotope effect (KH2O/KD2O)...Ch. 22 - Prob. 34PCh. 22 - Co2+ catalyzes the hydrolysis of the lactam shown...Ch. 22 - there are two kinds of aldolases. Class I...Ch. 22 - Prob. 37PCh. 22 - The hydrolysis of the ester shown here is...Ch. 22 - Prob. 39PCh. 22 - At pH = 12, the rate of hydrolysis of ester A is...Ch. 22 - 2-Acetoxycyclohexyl tosylate reacts with acetate...Ch. 22 - Proof that an imine was formed between aldolase...Ch. 22 - Prob. 43PCh. 22 - a. Explain why the alkyl halide shown here reacts...Ch. 22 - Triosephosphate isomerase (TIM) catalyzes the...
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