Reaction 1 H,C-C- CH, CH, HC-C- CH,CH, он A Reaction 2 H ex cess conc, H, SO, H,C-C-CH,CH, tut-1-ene and but-2-ene 180°C OH B When 5.0 g of butanone were used to carry out Reaction 1, the yield was 64% of the theoretical maximum. Calculate the mass of compound A formed. (a) (b) Given the table of infra-red absorption data below, describe the two maior differences between the infra-red spectra of butanone and of B. Table of infra-red absorption data Вond Wavenumber/em"! с —н C-C 2850-3300 C=C C=0 750-1100 1620-1680 1680-1750 C-0 1000–1300 3230-3550 0-H (alcohols) 0-H (acids) 2500-3000
Reaction 1 H,C-C- CH, CH, HC-C- CH,CH, он A Reaction 2 H ex cess conc, H, SO, H,C-C-CH,CH, tut-1-ene and but-2-ene 180°C OH B When 5.0 g of butanone were used to carry out Reaction 1, the yield was 64% of the theoretical maximum. Calculate the mass of compound A formed. (a) (b) Given the table of infra-red absorption data below, describe the two maior differences between the infra-red spectra of butanone and of B. Table of infra-red absorption data Вond Wavenumber/em"! с —н C-C 2850-3300 C=C C=0 750-1100 1620-1680 1680-1750 C-0 1000–1300 3230-3550 0-H (alcohols) 0-H (acids) 2500-3000
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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CN
Reaction 1
H;C-C- CH, CH,
HC-C-CH, CH;
OH
A
Reaction 2
H
ex cess
conc, H, SO,
H,C-C-CH,CH,
but-1-ene and but-2-ene
180°C
он
OH
B
(a)
When 5.0 g of butanone were used to carry out Reaction 1, the yield was 64% of the
theoretical maximum. Calculate the mass of compound A formed.
Given the table of infra-red absorption data below, describe the two major
differences between the infra-red spectra of butanone and of B.
(b)
Table of infra-red absorption data
Wavenumber/cm
Bond
С —Н
С — с
2850-3300
750-1100
C=C
1620-1680
C=0
с —о
о—Н (alcohols)
0-H (acids)
1680–1750
1000–1300
3230-3550
2500-3000
(c)
Draw the structure of the repeating unit in the polymer which can be formed from
Page 1 of 9
1315 words
LE English (United Kingdom) Accessibility: Unavailable
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Transcribed Image Text:AS - ALCOHOLS TEST PRACTICE 2021-2022 QP ONLY [Compatibility Mode] - Word
Mariella Dini
File
Home
Insert
Design
Layout
References
Mailings
Review
View
Help
O Tell me what you want to do
2 Share
X Cut
P Find -
Times New Roma -||11
-
A A Aa v
AABBCCI AABBCCI AaBbC AaBbC AaBbC AaBbCcD AABBCCL
ED Copy
ac Replace
E Select
Paste
BI U v abe x, x²
A
ay A -
I Normal I No Spac. Heading 1 Heading 2
Subtitle
Subtle Em..
Title
Format Painter
Clipboard
Font
Paragraph
Styles
Editing
CN
Reaction 1
H;C-C- CH, CH,
HC-C-CH, CH;
OH
A
Reaction 2
H
ex cess
conc, H, SO,
H,C-C-CH,CH,
but-1-ene and but-2-ene
180°C
он
OH
B
(a)
When 5.0 g of butanone were used to carry out Reaction 1, the yield was 64% of the
theoretical maximum. Calculate the mass of compound A formed.
Given the table of infra-red absorption data below, describe the two major
differences between the infra-red spectra of butanone and of B.
(b)
Table of infra-red absorption data
Wavenumber/cm
Bond
С —Н
С — с
2850-3300
750-1100
C=C
1620-1680
C=0
с —о
о—Н (alcohols)
0-H (acids)
1680–1750
1000–1300
3230-3550
2500-3000
(c)
Draw the structure of the repeating unit in the polymer which can be formed from
Page 1 of 9
1315 words
LE English (United Kingdom) Accessibility: Unavailable
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