Use the data in Table 7-2 to predict the energy difference between pent-1-ene and cis-pent-2-ene. Express your answer to two siginificant figures. VO Az ? 6.6 kJ/mol Submit Previous Answers Request Answer

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Predict the energy difference between pent-1-ene and cis-pent-2-ene.

Part A
Use the data in Table 7-2 to predict the energy difference between pent-1-ene and cis-pent-2-ene.
Express your answer to two siginificant figures.
?
6.6
kJ/mol
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Transcribed Image Text:Part A Use the data in Table 7-2 to predict the energy difference between pent-1-ene and cis-pent-2-ene. Express your answer to two siginificant figures. ? 6.6 kJ/mol Submit Previous Answers Request Answer X Incorrect; Try Again; 2 attempts remaining
TABLE 7-2
Molar Heats of Hydrogenation of Alkenes
Molar Heat of
Hydrogenation (-AH")
Name
Structure
kJ
kcal
General Structure
ethene (ethylene)
H,C=CH2
136.0
32.5}
unsubstituted
CH3-CH=CH,
CH3-CH CH=CH2
CH3-CH CH,-CH=CH2
CH3-(CH)3-CH=CH2
(CH3),CH-CH=CH2
(CH3),C-CH=CH2
propene (propylene)
123.4
29.5
but-1-ene
125.9
126.0
30.1
monosubstituted
pent-1-ene
hex-1-ene
30.1
125.0
R-CH=CH2
3-methylbut-1-ene
3,3-dimethylbut-1-ene
126.3
125.8
29.9
30.2
30.1
CH3
CH3
cis-but-2-ene
118.5
28.3
disubstituted (cis)
H
H.
R.
R
CH3-CH2
CH3
cis-pent-2-ene
117.7
28.1
H
H.
H
H.
2-methylpropene
(isobutylene)
2-methylbut-1-ene
(CH3),C=CH2
117.8
28.2
disubstituted (geminal)
CH3-CH2-C=CH2
118.2
28.3
R
c=CH2
R
ČH3
2,3-dimethylbut-1-ene
(CH3),CH-C=CH,
116.3
27.8
ČH3
CH3
H.
trans-but-2-ene
114.6
27.4
disubstituted (trans)
H
CH3
R
C=C
H
CH-CH2
H
trans-pent-2-ene
113.8
27.2
H
R
H
CH3
2-methylbut-2-ene
CH C=CH-CH3
111.6
trisubstituted
RC=CHR
ČH3
2,3-dimethylbut-2-ene
(CH3),C=C(CH3)2
110.4
26.4
tetrasubstituted
R,C=CR2
Note: A lower heat of hydrogenation corresponds to lower energy and greater stability of the alkene.
Transcribed Image Text:TABLE 7-2 Molar Heats of Hydrogenation of Alkenes Molar Heat of Hydrogenation (-AH") Name Structure kJ kcal General Structure ethene (ethylene) H,C=CH2 136.0 32.5} unsubstituted CH3-CH=CH, CH3-CH CH=CH2 CH3-CH CH,-CH=CH2 CH3-(CH)3-CH=CH2 (CH3),CH-CH=CH2 (CH3),C-CH=CH2 propene (propylene) 123.4 29.5 but-1-ene 125.9 126.0 30.1 monosubstituted pent-1-ene hex-1-ene 30.1 125.0 R-CH=CH2 3-methylbut-1-ene 3,3-dimethylbut-1-ene 126.3 125.8 29.9 30.2 30.1 CH3 CH3 cis-but-2-ene 118.5 28.3 disubstituted (cis) H H. R. R CH3-CH2 CH3 cis-pent-2-ene 117.7 28.1 H H. H H. 2-methylpropene (isobutylene) 2-methylbut-1-ene (CH3),C=CH2 117.8 28.2 disubstituted (geminal) CH3-CH2-C=CH2 118.2 28.3 R c=CH2 R ČH3 2,3-dimethylbut-1-ene (CH3),CH-C=CH, 116.3 27.8 ČH3 CH3 H. trans-but-2-ene 114.6 27.4 disubstituted (trans) H CH3 R C=C H CH-CH2 H trans-pent-2-ene 113.8 27.2 H R H CH3 2-methylbut-2-ene CH C=CH-CH3 111.6 trisubstituted RC=CHR ČH3 2,3-dimethylbut-2-ene (CH3),C=C(CH3)2 110.4 26.4 tetrasubstituted R,C=CR2 Note: A lower heat of hydrogenation corresponds to lower energy and greater stability of the alkene.
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