Question

Part A How many and bonds are present in a molecule of cumulene? (Part A 1...

cumulene.jpg



Part A 

How many \(\sigma\) and \(\pi\) bonds are present in a molecule of cumulene? (Part A 1 figure) Enter the number of \(\sigma\) bonds followed by the number of \(\pi\) bonds separated by a comma. 


Part B What types of orbital overlap occur incumulene? Check all that apply. \(s p^{2} / s p^{2}\) overlap


\(s p / s p^{2}\) overlap


\(s p / s p\) overlap


\(s / s\) overlap


\(s / s p^{2}\) overlap


\(p / p\) overlap \(s / s p\) overlap


In cumulene, what are the \(\mathrm{C}=\mathrm{C}=\mathrm{C}\) and \(\mathrm{H}-\mathrm{C}-\mathrm{H}\) bond angles, respectively? Enter the \(\mathrm{C}=\mathrm{C}=\mathrm{C}\) bond angle followed by the \(\mathrm{H}-\mathrm{C}-\mathrm{H}\) bond angle separated by a comma.

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Answer #1
Concepts and reason

The chemical bond is formed by the attraction of atom or ions. Due to electronegativity, the atoms can attract the electrons in a chemical bond. Chemical bond is also formed with the help of valance electrons in an atom and should obey octet rule.

The chemical bonding is formed with the help of overlapping of atomic orbitals.

There are two types of bond. They are sigma bond (σ)\left( \sigma \right) and pi bond (π)\left( {\rm{\pi }} \right) .

Fundamentals

Sigma bond:

The head – on overlapping of atomic orbitals which leads to covalent bond formation is represented as sigma bond.

Pi bond:

A side wise overlapping of atomic orbitals which leads to the formation of bond is represented as pi bond.

Example: H2C=
CH2

The double bond in ethene contains 1 sigma bond and 1 pi bond. The 4 electrons of each carbon forms a bond with 2 hydrogen, 1 carbon – carbon bond and 1 pi bond with carbon.

sidewise overlap it
head on overlapping
head on overlapping o

The double bond in ethene includes 1 σ(sp2sp2overlap){\rm{\sigma }}\,{\rm{(s}}{{\rm{p}}^{\rm{2}}}{\rm{ - s}}{{\rm{p}}^{\rm{2}}}{\rm{ overlap)}} and 1 π(ppoverlap){\rm{\pi }}\,{\rm{(p}}\,{\rm{ - }}\,{\rm{p overlap)}} bonds. Each carbon – hydrogen bond shows σ(sp2soverlap){\rm{\sigma }}\,{\rm{(s}}{{\rm{p}}^{\rm{2}}}{\rm{ - s overlap)}} .The bond angle is 1200 and shows Trigonal planar geometry.

(A)

HO
I
6
TTTTTT
C
C7
I
HOOT

(B.1)

CECECEC

The corner carbon (red) shows sp2{\rm{s}}{{\rm{p}}^{\rm{2}}} hybridization and the two carbons present in the center (blue) shows sp{\rm{sp}} hybridization. Each hydrogen contains s{\rm{s}} orbital which undergoes head – on overlapping with carbon atom.

The two carbons in the corner that shows sp2{\rm{s}}{{\rm{p}}^{\rm{2}}} hybridization and bonds with carbons are sp{\rm{sp}} hybridized. Therefore, there is no sp2/sp2{\rm{s}}{{\rm{p}}^{\rm{2}}}{\rm{/s}}{{\rm{p}}^{\rm{2}}} overlap in this molecule.

The hydrogen present in this molecule has s{\rm{s}} orbital which bonds with sp2{\rm{s}}{{\rm{p}}^{\rm{2}}} carbon. Therefore, there is no s/s{\rm{s/s}} overlap in this molecule.

The hydrogen present in this molecule has s{\rm{s}} orbital which is bonded with sp2{\rm{s}}{{\rm{p}}^{\rm{2}}} carbon. There is no s{\rm{s}} orbital overlap with sp{\rm{sp}} carbon. Therefore, there is no s/sp{\rm{s/sp}} overlap present in this molecule.

The carbon present in the center shows sp{\rm{sp}} hybridization and the carbon present in the corner shows sp2{\rm{s}}{{\rm{p}}^{\rm{2}}} hybridization. Therefore, the molecule has sp/sp2{\rm{sp /s}}{{\rm{p}}^{\rm{2}}} overlap.

(B.2)

CECECEC

sp/spoverlap{\rm{sp/sp overlap}}

(B.3)

C=
C=
C=
C

Cumulene molecule shows s/sp2{\rm{s /s}}{{\rm{p}}^2} overlap.

(B.4)

C=
C=
C=
C

Cumulene molecule shows p/p{\rm{p / p}} overlap.

1800
Hc<=
=CH2

120° CECECEC

Ans: Part A

Cumulene contains 7 sigma bond and 3 pi bonds.

Part B.1

O

sp2/sp2{\rm{s}}{{\rm{p}}^2}{\rm{ /s}}{{\rm{p}}^{\rm{2}}} overlap

O

sp/sp2{\rm{sp /s}}{{\rm{p}}^{\rm{2}}} overlap

O

sp/sp{\rm{sp /sp}} overlap

O

s/s{\rm{s /s}} overlap

O

s/sp2{\rm{s /s}}{{\rm{p}}^{\rm{2}}} overlap

O

p/p{\rm{p /p}} overlap

O

s/sp{\rm{s /sp}} overlap

Part B.2

O

sp2/sp2{\rm{s}}{{\rm{p}}^2}{\rm{ /s}}{{\rm{p}}^{\rm{2}}} overlap

O

sp/sp2{\rm{sp /s}}{{\rm{p}}^{\rm{2}}} overlap

O

sp/sp{\rm{sp /sp}} overlap

O

s/s{\rm{s /s}} overlap

O

s/sp2{\rm{s /s}}{{\rm{p}}^{\rm{2}}} overlap

O

p/p{\rm{p /p}} overlap

O

s/sp{\rm{s /sp}} overlap

Part B.3

O

sp2/sp2{\rm{s}}{{\rm{p}}^2}{\rm{ /s}}{{\rm{p}}^{\rm{2}}} overlap

O

sp/sp2{\rm{sp /s}}{{\rm{p}}^{\rm{2}}} overlap

O

sp/sp{\rm{sp /sp}} overlap

O

s/s{\rm{s /s}} overlap

O

s/sp2{\rm{s /s}}{{\rm{p}}^{\rm{2}}} overlap

O

p/p{\rm{p /p}} overlap

O

s/sp{\rm{s /sp}} overlap

Part B.4

O

sp2/sp2{\rm{s}}{{\rm{p}}^2}{\rm{ /s}}{{\rm{p}}^{\rm{2}}} overlap

O

sp/sp2{\rm{sp /s}}{{\rm{p}}^{\rm{2}}} overlap

O

sp/sp{\rm{sp /sp}} overlap

O

s/s{\rm{s /s}} overlap

O

s/sp2{\rm{s /s}}{{\rm{p}}^{\rm{2}}} overlap

O

p/p{\rm{p /p}} overlap

O

s/sp{\rm{s /sp}} overlap

H2C=
C=
C=CH2
, =
=
C=
C

The bond angle is 1800,1200.{180^0}\,,\,{120^0}.

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