EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
9th Edition
ISBN: 9780136781776
Author: Wade
Publisher: PEARSON CO
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Textbook Question
Chapter 12.3, Problem 12.1P
Complete the following conversion table.
|
|
4000 | 1700 | 1640 | 1600 | 400 | |||
| λ(μm) | 2.50 | 3.03 | 3.33 | 4.55 | 25.0 |
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3. Is 2-methyl-2-propanol a primary, secondary, or tertiary alcohol? Write
out the
structures of 2-methyl-2-propanol and also any oxidation products of 2-
methyl-2-
propanol. If there is more than one oxidation product, give the structure of
each
of the products.
4. 2-Propanol is the IUPAC systematic name of this alcohol. It has a
common name
by which it is much better known (You'll see it in the grocery store or
pharmacy).
Give that common name
5. Aldehydes can be synthesized by the oxidation of. Please choose from
below choices
A. Primary alcohols
B. Secondary alcohols
C. Organic acids
D. Inorganic acids
6. Tertiary alcohol Can undergo oxidation. yes or no. ? If yes then answer the
product.
Finish the reactions
hand written please
Part A
Identify each alcohol as primary, secondary, or tertiary
Drag the appropriate items to their respective bins.
CH₂
H₂C-
-C-OH
HO
CH₂
Primary
Он
OH
CH₂
OH
CCH₂OH
CH₂
сн
Secondary
Tertiary
Reset Help
CH,CH₂
(CH)CHCH,OH CH,CH,CH,CCH,
CHOH
CH₂
Different types of alcohol groups
Alcohol and its reaction:
8. Combing two alcohol molecules below and completing the reaction with
Product .( Hint Reaction called etherification as ether is formed and name the
ether once you complete the reaction.
Hint.:
R-O-H+H-O-RR-O-R
Do the reaction:
CH₂OH + CH₂OH---→
+ H-O-H
9. Write the reaction of formation of alcohol from alkene by adding water:
Addition reaction also called hydration reaction as we are adding water
which occur always in presence of acid
Hint: Break the double bond and add H and OH if symmetrical then
add anywhere if unsymmetrical then follow Markovnikov rule H
should go to that double bone carbon which has more hydrogen
CH2=CH2 + H₂O-→
Chapter 12 Solutions
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
Ch. 12.3 - Complete the following conversion table. (cm1)...Ch. 12.5 - Which of the bonds shown in red are expected to...Ch. 12.7C - For each hydrocarbon spectrum, determine whether...Ch. 12.9A - Spectra are given for three compounds. Each...Ch. 12.10 - The infrared spectra for three compounds are...Ch. 12.12 - Prob. 12.6PCh. 12.14B - Identify which of these four mass spectra indicate...Ch. 12.15A - Show the fragmentation that accounts for the...Ch. 12.15A - Show the fragmentations that give rise to the...Ch. 12.15B - Ethers are not easily differentiated by their...
Ch. 12.15C - Prob. 12.11PCh. 12 - Prob. 12.12SPCh. 12 - Prob. 12.13SPCh. 12 - All of the following compounds absorb infrared...Ch. 12 - Prob. 12.15SPCh. 12 - Four infrared spectra are shown, corresponding to...Ch. 12 - Predict the masses and the structures of the most...Ch. 12 - Prob. 12.18SPCh. 12 - Prob. 12.19SPCh. 12 - (A true story) While organizing the undergraduate...Ch. 12 - Prob. 12.21SPCh. 12 - Prob. 12.22SPCh. 12 - An unknown, foul-smelling hydrocarbon gives the...Ch. 12 - covered a synthesis of alkynes by a double...Ch. 12 - Three IR spectra are shown, corresponding to three...Ch. 12 - Prob. 12.26SPCh. 12 - Prob. 12.27SPCh. 12 - Prob. 12.28SPCh. 12 - The ultimate test of fluency in MS and IR is...Ch. 12 - Prob. 12.30SPCh. 12 - Consider the following four structures, followed...
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