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Concept explainers
For alanine,
(a) 2.00.
(b) 6.00.
(c) 10.50.
What is the principal species at each pH?
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(a)
Interpretation:
The value of
Concept introduction:
General formula of alanine is shown as follows:
The
Answer to Problem 29QAP
The principal species at
Explanation of Solution
Under equilibrium condition, the Zwitter ionic form of alanine is shown as follows:
Under acidic condition, oxygen atom accepts the proton Zwitter ion exists in cationic form.
Under basic condition, base abstracts proton form nitrogen atom and it forms the anionic form.
Dissociation of cation is represented as follows:
Dissociation of anion is represented as follows:
Given value of
At
So,
Take antilog both sides,
Here, Z is Zwitter ion and C is cationic form of Zwitter ion.
Here, Z is Zwitter ion and A is anionic form of Zwitter ion.
Therefore,
The principal species at
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(b)
Interpretation:
The value of
Concept introduction:
General formula of alanine is shown as follows:
The
Answer to Problem 29QAP
The principal species at
Explanation of Solution
Under equilibrium condition zwitter ionic form of alanine is:
Under acidic condition oxygen atom accepts the proton zwitter ion exists in cationic form.
Under basic condition base abstracts proton form nitrogen atom and it forms the anionic form.
Dissociation of cation is-
Dissociation of anion is-
Given value of
At
So,
Take antilog both sides,
Here, Z is zwitter ion and C is cationic form of zwitter ion.
Here, Z is zwitter ion and A is anionic form of zwitter ion.
The principal species at
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(c)
Interpretation:
The value of
Concept introduction:
General formula of alanine is shown as follows:
The
Answer to Problem 29QAP
The principal species at
Explanation of Solution
Under equilibrium condition zwitter ionic form of alanine is:
Under acidic condition oxygen atom accepts the proton zwitter ion exists in cationic form.
Under basic condition base abstracts proton form nitrogen atom and it forms the anionic form.
Dissociation of cation is-
Dissociation of anion is-
Given value of
At
So,
Take antilog both sides,
Here, Z is zwitter ion and C is cationic form of zwitter ion.
Here, Z is zwitter ion and A is anionic form of zwitter ion.
The principal species at
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Chapter 23 Solutions
OWLv2 with Student Solutions Manual eBook for Masterton/Hurley's Chemistry: Principles and Reactions, 8th Edition, [Instant Access], 4 terms (24 months)
- Identify the missing organic reactants in the following reaction: X + Y H+ two steps Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forwardI need help naming these in IUPACarrow_forward
- H R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centearrow_forwardDraw the friedel-crafts acylation mechanism of m-Xylenearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- 1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products? 2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?arrow_forwardExplain Huckel's rule.arrow_forwardhere is my question can u help me please!arrow_forward
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