A chemical equation for the given information has to be written and the conjugate acid, base has to be identified. Concept introduction: Acid: According to Bronsted-Lowry theory, a species which donates a proton in a proton transfer-reaction is said to be an acid. Base: According to Bronsted-Lowry theory, a species which accepts a proton in a proton transfer-reaction is said to be base. Conjugated acid: In the conjugate acid-base pair, a species which can donates a proton is said to be conjugated acid. Conjugated base: In the conjugate acid-base pair, a species which can accepts a proton is said to be conjugated base.
A chemical equation for the given information has to be written and the conjugate acid, base has to be identified. Concept introduction: Acid: According to Bronsted-Lowry theory, a species which donates a proton in a proton transfer-reaction is said to be an acid. Base: According to Bronsted-Lowry theory, a species which accepts a proton in a proton transfer-reaction is said to be base. Conjugated acid: In the conjugate acid-base pair, a species which can donates a proton is said to be conjugated acid. Conjugated base: In the conjugate acid-base pair, a species which can accepts a proton is said to be conjugated base.
Author: Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
The conjugate acid-base pairs are ([Al(H2O)6]3+,[Al(H2O)5OH]2+ ) and (NH4+,NH3)
Explanation of Solution
The hydrated aluminum ion acts as Bronsted-Lowry acid and it can react with ammonia a Bronsted-Lowry base to produce as mentioned ions in the following reaction.
The conjugate acid-base pairs are (CH3CH2SH2+, CH3CH2SH) and (H2SO4,HSO4-)
Explanation of Solution
Ethanethiol acts as Bronsted-Lowry base and it can react with sulfuric acid a Bronsted-Lowry acid to produce as mentioned ions in the following reaction.
Michael Reactions
19.52 Draw the products from the following Michael addition reactions.
1.
H&C CH
(a)
i
2. H₂O*
(b)
OEt
(c)
EtO
H₂NEt
(d)
ΕΙΟ
+
1. NaOEt
2. H₂O'
H
H
1. NaOEt
2. H₂O*
Rank the labeled protons (Ha-Hd) in order of increasing acidity, starting with the least acidic.
НОН НЬ
OHd
Онс
Can the target compound at right be efficiently synthesized in good yield from the unsubstituted benzene at left?
?
starting
material
target
If so, draw a synthesis below. If no synthesis using reagents ALEKS recognizes is possible, check the box under the drawing area.
Be sure you follow the standard ALEKS rules for submitting syntheses.
+ More...
Note for advanced students: you may assume that you are using a large excess of benzene as your starting material.
C
:0
T
Add/Remove step
G
Chapter 15 Solutions
General Chemistry - Standalone book (MindTap Course List)
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Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell