In Exercise 89 in Chapter 3, the Lewis structures for benzene (C 6 H 6 ) were drawn. Using one of the Lewis Structures, estimate Δ H f ° for C 6 H 6 ( g ) using bond energies and given that the standard enthalpy of formation of C(g) is 717 kJ/mol. The experimental Δ H f ° value for C 6 H 6 ( g ) is 83 kJ/mol. Explain the discrepancy between the experimental value and the calculated Δ H f ° value for C 6 H 6 ( g ).
In Exercise 89 in Chapter 3, the Lewis structures for benzene (C 6 H 6 ) were drawn. Using one of the Lewis Structures, estimate Δ H f ° for C 6 H 6 ( g ) using bond energies and given that the standard enthalpy of formation of C(g) is 717 kJ/mol. The experimental Δ H f ° value for C 6 H 6 ( g ) is 83 kJ/mol. Explain the discrepancy between the experimental value and the calculated Δ H f ° value for C 6 H 6 ( g ).
Solution Summary: The author explains that the standard enthalpy of formation should be calculated and the reason for experimental value is lesser than the calculated value has to be explained.
In Exercise 89 in Chapter 3, the Lewis structures for benzene (C6H6) were drawn. Using one of the Lewis Structures, estimate
Δ
H
f
°
for C6H6(g) using bond energies and given that the standard enthalpy of formation of C(g) is 717 kJ/mol. The experimental
Δ
H
f
°
value for C6H6 (g) is 83 kJ/mol. Explain the discrepancy between the experimental value and the calculated
Δ
H
f
°
value for C6H6(g).
19. (3 pts) in Chapter 7 we will see a reaction of halocyclohexanes that requires that the halogen occupy an axial position with
this in mind, would you expect cis-1-bromo-3-methylcyclohexane or trans-1-bromo-3-methylcyclohexane to be more
reactive in this reaction? Briefly explain your choice using structures to support your answer.
Mere-eries-cecleone)
The tran-i-browse-3-methylcyclohexione
Please help me calculate the undiluted samples ppm concentration.
My calculations were 280.11 ppm. Please see if I did my math correctly using the following standard curve.
Link: https://mnscu-my.sharepoint.com/:x:/g/personal/vi2163ss_go_minnstate_edu/EVSJL_W0qrxMkUjK2J3xMUEBHDu0UM1vPKQ-bc9HTcYXDQ?e=hVuPC4
Provide an IUPAC name for each of the compounds shown.
(Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to
commas, dashes, etc.)
H₁₂C
C(CH3)3
C=C
H3C
CH3
CH3CH2CH
CI
CH3
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