Ethylene glycol, HOCH 2 CH 2 OH, is used as antifreeze. It is produced from ethylene oxide, C 2 H 4 O, by the reaction C 2 H 4 O ( g ) + H 2 O ( l ) → HOCH 2 CH 2 OH ( l ) Use Hess’s law to obtain the enthalpy change for this reaction from the following enthalpy changes: 2 C 2 H 4 O ( g ) + 5 O 2 ( g ) → 4 CO 2 ( g ) + 4 H 2 O ( l ) ; Δ H = − 2612.2 kJ HOCH 2 CH 2 OH ( l ) + 5 2 O 2 ( g ) → 2 CO 2 ( g ) + 3 H 2 O ( l ) ; Δ H = − 1189.8 kJ
Ethylene glycol, HOCH 2 CH 2 OH, is used as antifreeze. It is produced from ethylene oxide, C 2 H 4 O, by the reaction C 2 H 4 O ( g ) + H 2 O ( l ) → HOCH 2 CH 2 OH ( l ) Use Hess’s law to obtain the enthalpy change for this reaction from the following enthalpy changes: 2 C 2 H 4 O ( g ) + 5 O 2 ( g ) → 4 CO 2 ( g ) + 4 H 2 O ( l ) ; Δ H = − 2612.2 kJ HOCH 2 CH 2 OH ( l ) + 5 2 O 2 ( g ) → 2 CO 2 ( g ) + 3 H 2 O ( l ) ; Δ H = − 1189.8 kJ
Ethylene glycol, HOCH2CH2OH, is used as antifreeze. It is produced from ethylene oxide, C2H4O, by the reaction
C
2
H
4
O
(
g
)
+
H
2
O
(
l
)
→
HOCH
2
CH
2
OH
(
l
)
Use Hess’s law to obtain the enthalpy change for this reaction from the following enthalpy changes:
2
C
2
H
4
O
(
g
)
+
5
O
2
(
g
)
→
4
CO
2
(
g
)
+
4
H
2
O
(
l
)
;
Δ
H
=
−
2612.2
kJ
HOCH
2
CH
2
OH
(
l
)
+
5
2
O
2
(
g
)
→
2
CO
2
(
g
)
+
3
H
2
O
(
l
)
;
Δ
H
=
−
1189.8
kJ
Draw a Lewis structure for each of the following molecules and assign
charges where appropriate. The order in which the atoms are connected
is given in parentheses.
a. CIFCIF
b. BrCNBrCN
0
c. SOCI2 × (CISCIO) SOC₁₂ (CISCI)
You can draw both an octet and a valence
shell expanded structure. Considering the following structural information, which
is the better one: The measured S-OS-O bond length in SOC12SOCl2 is 1.43 Å.
For comparison, that in SO2SO2 is 1.43 Å [Exercise 1-9, part (b)], that in
CHзSOHCH3 SOH
d. CH3NH2CH3NH2
(methanesulfenic acid) is 1.66 A.
e. CH3OCH3 CH3 OCH3
NH2
f. N2H2× (HNNH) N2 H2 (HNNH)
g. CH2COCH₂ CO
h. HN3× (HNNN) HN3 (HNNN)
i. N20 × (NNO) N2O (NNO)
bre
The reaction sequence shown in Scheme 5 demonstrates the synthesis of a
substituted benzene derivative Q.
wolsd works 2
NH2
NaNO2, HCI
(apexe) 13× (1
HNO3, H2SO4
C6H5CIN2
0°C
HOTE
CHINO₂
N
O
*O₂H (
PO
Q
Я
Scheme 5
2 bag abouoqmics to sounde odi WEIC
(i)
Draw the structure of intermediate O.
[2 marks]
to noitsmot od: tot meinedogm, noit so oft listsb ni zaupaib bas wa
(ii) Draw the mechanism for the transformation of aniline N to intermediate O.
Spoilage
(b)
[6 marks]
(iii) Identify the reagent X used to convert compound O to the iodinated compound
[tom E
P.
vueimado oilovonsa ni moitos nolisbnolov ayd toes ai tedw nisiqx
(iv) Identify the possible structures of compound Q.
[2 marks]
[2 marks]
[shom 2]
(v)
bus noires goiribbeolovo xnivollot adj to subora sidab
Draw the mechanism for the transformation of intermediate P to compound Q.
[5 marks]
vi
(vi) Account for the regiochemical outcome observed in the reaction forming
compound Q.
[3 marks]
PROBLEM 4 Solved
Show how 1-butanol can be converted into the following compounds:
a.
PROBLEM 5+
b.
d.
-C=
N
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Calorimetry Concept, Examples and Thermochemistry | How to Pass Chemistry; Author: Melissa Maribel;https://www.youtube.com/watch?v=nSh29lUGj00;License: Standard YouTube License, CC-BY