Be sure to answer all parts. Compound A exhibits a peak in its 'H NMR spectrum at 7.6 ppm, indicating that it is aromatic. absorbs at 7.6 ppm A = In order to make the molecular orbitals, how must the atomic orbitals on the carbons that comprise the triple bonds be hybridized? A. sp O B. sp OC. sp In what type of orbitals are the a electrons of the triple bonds contained? O A. d orbitals O B. p orbitals c. s orbitals How many n electrons are delocalized around the ring in A? electrons

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Chapter1: Chemical Foundations
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Be sure to answer all parts.
Compound A exhibits a peak in its 'H NMR spectrum at 7.6 ppm, indicating that it is aromatic.
absorbs at 7.6 ppm
A =
In order to make the molecular orbitals, how must the atomic orbitals on the carbons that comprise the
triple bonds be hybridized?
O A. sp
O B. sp
В.
O C.
sp
In what type of orbitals are the a electrons of the triple bonds contained?
O A.
d orbitals
O B.
p orbitals
s orbitals
How many n electrons are delocalized around the ring in A?
electrons
Transcribed Image Text:Be sure to answer all parts. Compound A exhibits a peak in its 'H NMR spectrum at 7.6 ppm, indicating that it is aromatic. absorbs at 7.6 ppm A = In order to make the molecular orbitals, how must the atomic orbitals on the carbons that comprise the triple bonds be hybridized? O A. sp O B. sp В. O C. sp In what type of orbitals are the a electrons of the triple bonds contained? O A. d orbitals O B. p orbitals s orbitals How many n electrons are delocalized around the ring in A? electrons
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