Organic Chemistry, Third Edition Binder Ready Version
3rd Edition
ISBN: 9781119110453
Author: Klein
Publisher: WILEY
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Question
Chapter 12.10, Problem 21ATS
Interpretation Introduction
Interpretation:
An efficient synthesis for conversion of compound 1 to 2 has to be provided.
Concept Introduction:
- Hydroboration-oxidation reaction: Addition of
- Oxidation: Oxidation involves loss of electrons. In organic chemistry, oxidation is removal of hydrogen ad addition of oxygen. There are substance which oxidizes other substance and get reduces itself are called oxidising agent. Example: chromium oxide.
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Students have asked these similar questions
1. Consider the following molecular-level diagrams of a titration.
O-HA molecule
-Aion
°°
о
°
(a)
о
(b)
(c)
(d)
a. Which diagram best illustrates the microscopic representation for the
EQUIVALENCE POINT in a titration of a weak acid (HA) with sodium.
hydroxide?
(e)
Answers to the remaining 6 questions will be hand-drawn on paper and submitted as a single
file upload below:
Review of this week's reaction:
H₂NCN (cyanamide) + CH3NHCH2COOH (sarcosine) + NaCl, NH4OH, H₂O --->
H₂NC(=NH)N(CH3)CH2COOH (creatine)
Q7. Draw by hand the reaction of creatine synthesis listed above using line structures without showing
the Cs and some of the Hs, but include the lone pairs of electrons wherever they apply. (4 pts)
Q8. Considering the Zwitterion form of an amino acid, draw the Zwitterion form of Creatine. (2 pts)
Q9. Explain with drawing why the C-N bond shown in creatine structure below can or cannot rotate. (3
pts)
NH2(C=NH)-N(CH)CH2COOH
This bond
Q10. Draw two tautomers of creatine using line structures. (Note: this question is valid because problem
Q9 is valid). (4 pts)
Q11. Mechanism. After seeing and understanding the mechanism of creatine synthesis, students should
be ready to understand the first half of one of the Grignard reactions presented in a past…
Propose a synthesis pathway for the
following transformations. b) c) d)
Chapter 12 Solutions
Organic Chemistry, Third Edition Binder Ready Version
Ch. 12.1 - Prob. 1LTSCh. 12.1 - PRACTICE the skill
Provide an IUPAC name for each...Ch. 12.1 - Safer alternatives to existing insecticides and...Ch. 12.1 - Prob. 3CCCh. 12.2 - Prob. 4CCCh. 12.2 - Prob. 2LTSCh. 12.2 - Prob. 5PTSCh. 12.2 - Flavonoids are a class of naturally occurring...Ch. 12.3 - Prob. 7CCCh. 12.3 - Prob. 8CC
Ch. 12.4 - Prob. 3LTSCh. 12.4 - Prob. 9PTSCh. 12.4 - Prob. 10ATSCh. 12.4 - Prob. 4LTSCh. 12.4 - Prob. 11PTSCh. 12.4 - Prob. 12ATSCh. 12.6 - Prob. 5LTSCh. 12.6 - Prob. 13PTSCh. 12.6 - Prob. 14PTSCh. 12.7 - Prob. 16CCCh. 12.9 - Prob. 6LTSCh. 12.9 - Prob. 17PTSCh. 12.9 - Prob. 18ATSCh. 12.9 - Prob. 19CCCh. 12.10 - Prob. 7LTSCh. 12.10 - PRACTICE the skill
Predict the major organic...Ch. 12.10 - Prob. 21ATSCh. 12.13 - Prob. 8LTSCh. 12.13 - Prob. 22PTSCh. 12.13 - Prob. 23ATSCh. 12.13 - Prob. 24CCCh. 12.13 - Prob. 9LTSCh. 12.13 - Prob. 25PTSCh. 12.13 - Prob. 26ATSCh. 12 - Prob. 27PPCh. 12 - Prob. 28PPCh. 12 - Prob. 29PPCh. 12 - Prob. 30PPCh. 12 - Prob. 31PPCh. 12 - Predict the major product of the reaction between...Ch. 12 - Prob. 33PPCh. 12 - Prob. 34PPCh. 12 - Using a Grignard reaction, show how you could...Ch. 12 - Each of the following alcohols can be prepared via...Ch. 12 - Prob. 37PPCh. 12 - Prob. 38PPCh. 12 - Prob. 39PPCh. 12 - Prob. 40PPCh. 12 - Prob. 41PPCh. 12 - Prob. 42PPCh. 12 - Prob. 43PPCh. 12 - Prob. 44PPCh. 12 - Prob. 45PPCh. 12 - Prob. 46PPCh. 12 - Prob. 47PPCh. 12 - Prob. 48PPCh. 12 - Prob. 49PPCh. 12 - Prob. 50PPCh. 12 - Prob. 51IPCh. 12 - Prob. 52IPCh. 12 - Prob. 53IPCh. 12 - Prob. 54IPCh. 12 - Prob. 55IPCh. 12 - Prob. 56IPCh. 12 - Prob. 57IPCh. 12 - Prob. 58IPCh. 12 - Prob. 59IPCh. 12 - Prob. 60IPCh. 12 - Prob. 61IPCh. 12 - Prob. 62IPCh. 12 - Prob. 63IPCh. 12 - Prob. 64IPCh. 12 - Prob. 65IPCh. 12 - The compound duryne was one of several...Ch. 12 - Estragole is an insect repellant that has been...Ch. 12 - Prob. 68IPCh. 12 - Prob. 70IPCh. 12 - Prob. 71IPCh. 12 - Prob. 72IPCh. 12 - Prob. 73IPCh. 12 - Prob. 74IPCh. 12 - Prob. 75CPCh. 12 - Prob. 76CPCh. 12 - Prob. 77CP
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