Acrylonitrile is the starting material used in the manufactureof acrylic fibers (U.S. annual production capacityis more than 2 million pounds). Three industrial processesfor the production of acrylonitrile are given below.Using data from Appendix 4, calculate Δ S °, Δ H °, and Δ G ° for each process. For part a, assume that T = 25 ° C ; for part b, T = 70. ° C ; and for part c, T = 700. ° C . Assume that Δ H ° and Δ S ° do not depend ontemperature. b. HC ≡ CH ( g ) + HCN ( g ) → 70 ° C-90°C CaCl 2 ⋅ HCl CH 2 = CHCN ( g ) c. 4HC 2 = CHCH 3 ( g ) + 6NO ( g ) → Ag 700 ° C CH 2 = CHCN ( g ) + 6 H 2 O ( g ) + N 2 ( g )
Acrylonitrile is the starting material used in the manufactureof acrylic fibers (U.S. annual production capacityis more than 2 million pounds). Three industrial processesfor the production of acrylonitrile are given below.Using data from Appendix 4, calculate Δ S °, Δ H °, and Δ G ° for each process. For part a, assume that T = 25 ° C ; for part b, T = 70. ° C ; and for part c, T = 700. ° C . Assume that Δ H ° and Δ S ° do not depend ontemperature. b. HC ≡ CH ( g ) + HCN ( g ) → 70 ° C-90°C CaCl 2 ⋅ HCl CH 2 = CHCN ( g ) c. 4HC 2 = CHCH 3 ( g ) + 6NO ( g ) → Ag 700 ° C CH 2 = CHCN ( g ) + 6 H 2 O ( g ) + N 2 ( g )
Solution Summary: The author explains the relationship between standard Gibbs free energy change, standard enthalpy change and Standard Entropy Change.
Acrylonitrile is the starting material used in the manufactureof acrylic fibers (U.S. annual production capacityis more than 2 million pounds). Three industrial processesfor the production of acrylonitrile are given below.Using data from Appendix 4, calculate
Δ
S
°,
Δ
H
°, and
Δ
G
°
for each process. For part a, assume that
T
=
25
°
C
; for part b,
T
=
70.
°
C
; and for part c,
T
=
700.
°
C
. Assume that
Δ
H
°
and
Δ
S
°
do not depend ontemperature. b.
HC
≡
CH
(
g
)
+
HCN
(
g
)
→
70
°
C-90°C
CaCl
2
⋅
HCl
CH
2
=
CHCN
(
g
)
c.
4HC
2
=
CHCH
3
(
g
)
+
6NO
(
g
)
→
Ag
700
°
C
CH
2
=
CHCN
(
g
)
+
6
H
2
O
(
g
)
+
N
2
(
g
)
Draw the Haworth projection of the disaccharide made by joining D-glucose and D-mannose with a ẞ(1-4) glycosidic bond. If the disaccharide has more than
one anomer, you can draw any of them.
Click and drag to start drawing a
structure.
X
Epoxides can be opened in aqueous acid or aqueous base to produce diols (molecules with two OH groups). In this question, you'll explore the
mechanism of epoxide opening in aqueous acid.
2nd attempt
Be sure to show all four bonds at stereocenters using hash and wedge lines.
0
0
Draw curved arrows to show how the epoxide reacts with hydronium ion.
100 +1:
1st attempt
Feedback
Be sure to show all four bonds at stereocenters using hash and wedge lines.
See Periodic Table
See Hint
H
A
5
F
F
Hr
See Periodic Table See Hint
03 Question (1 point)
For the reaction below, draw both of the major organic products. Be sure to consider stereochemistry.
>
1. CH₂CH₂MgBr
2. H₂O
3rd attempt
Draw all four bonds at chiral centers. Draw all stereoisomers formed.
Draw the structures here.
e
130
AN
H
See Periodic Table See Hint
P
C
Br
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