ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
10th Edition
ISBN: 9781259972348
Author: Carey
Publisher: MCG CUSTOM
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Chapter 9, Problem 38DSP
Interpretation Introduction
Interpretation:
The selection of the compound that describes thereaction mechanism that takes place in the first step of the given reaction is to be determined.
Concept Introduction:
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1
The structural prefix s- or sec- (for secondary-) and t- to tert- (for tertiary-) maybe incorporated in a
name to designate a specific secondary or tertiary alkyl group, respectively. If no isomeric alkyl group of the same
classification are possible. These prefixes are underlined italics and separated from the rest of the name by hyphens.
The alkyl group represented by formula
H3C
CH2 CH3
CH3
Xs named as
The parent chain in the compound
Contains
C atoms hence the alkene name for this parent chain is
properly numbered. The functional group is assigned the position number
the position number.
functional group is
When the parent chain is
and the substituents are assigned
- The complete designation of the parent chain, including the position of the
and
- The complete name of the formula is
1,2-dienes are classified as cumulated dienes, 1,3-dienes are conjugated dienes, and dienes that are separated by
one or more sp' hybridized carbon isolated dienes.
3…
Ethers can be prepared by reaction of an alkoxide or phenoxide ion with a primary alkyl halide.
Draw the structure of the expected organic product of the reaction of iodomethane with the following alkoxide ion:
CH3
H3C
O Na
You do not have to consider stereochemistry.
You do not have to explicitly draw H atoms.
• Do not include lone pairs in your answer. They will not be considered in the grading.
• Do not include counter-ions, e.g., Na", I, in your answer.
орy вste
ChemDoodle
4.) HX is used as a reagent in the reaction below.
„NH2
он +
HX
+ :NEN:
+
A. What functional-group transformation occurs in this reaction?
Chapter 9 Solutions
ORGANIC CHEMISTRY (LL)-W/SOLN.>CUSTOM<
Ch. 9.1 - Prob. 1PCh. 9.2 - Prob. 2PCh. 9.4 - How do bond distances and bond strengths change...Ch. 9.5 - Complete each of the following equations to show...Ch. 9.6 - Prob. 5PCh. 9.6 - Which of the alkynes of molecular formula C5H8 can...Ch. 9.7 - Give the structures of three isomeric dibromides...Ch. 9.7 - Prob. 8PCh. 9.9 - Write a series of equations showing how you could...Ch. 9.9 - Write a series of equations showing how to prepare...
Ch. 9.10 - Prob. 11PCh. 9.11 - Give the structure of the enol formed by hydration...Ch. 9.11 - Prob. 13PCh. 9.13 - Prob. 14PCh. 9.14 - Prob. 15PCh. 9 - Provide the IUPAC name for each of the following...Ch. 9 - Prob. 17PCh. 9 - All compounds in Problem 9.17 are isomers except...Ch. 9 - Prob. 19PCh. 9 - Write structural formulas for all the alkynes of...Ch. 9 - Prob. 21PCh. 9 - Prob. 22PCh. 9 - The alkane formed by hydrogenation of...Ch. 9 - Write the structure of the major organic product...Ch. 9 - Write the structure of the major organic product...Ch. 9 - When 2-heptyne was treated with aqueous sulfuric...Ch. 9 - Prob. 27PCh. 9 - Prob. 28PCh. 9 - Prob. 29PCh. 9 - Show by writing appropriate chemical equations how...Ch. 9 - Show by writing appropriate chemical equations how...Ch. 9 - Diphenylacetylene can be synthesized by the double...Ch. 9 - (Z)-9-tricosene [ (Z)-CH3(CH2)7CH=CH(CH2)12CH3 ]...Ch. 9 - Prob. 34PCh. 9 - Prob. 35PCh. 9 - Prob. 36PCh. 9 - Alkynes undergo hydroboration to give...Ch. 9 - Prob. 38DSPCh. 9 - Prob. 39DSPCh. 9 - Prob. 40DSPCh. 9 - Prob. 41DSPCh. 9 - Thinking Mechanistically About Alkynes The...
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