Question

In terms of hybridisation, bonding and stereochemistry, explain why alkenes are more chemically reactive than alkanes.

In terms of hybridisation, bonding and stereochemistry, explain why alkenes are more chemically reactive than alkanes.

Homework Answers

Answer #1

The high amount of P character in SP3 hybridized orbitals of the carbon in an alkane allows for more electron density to be aligned along the bond tragectory within the alkane

thus it forms strong and stable covalent bonds basically known as Sigma bonds ( single bonds).

Alkenes are SP2 hybridized and in SP2 hybridized orbitalsm more election density is situated around the core of the carbon nucleus and the pi orbitals in the pi bond are high in energy and therefore they are more available for bonding than electrons locked up in a sigma bond. There is also a steric factor as the SP2 system adopts an exposed planar structure.

So in conclusion energy required to break Sigma bond is more compared to pi bond. So double bond breaks easily in alkenes so they are less stable.

Know the answer?
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for?
Ask your own homework help question
Similar Questions
Explain why borazine is more reactive than benzene toward the addition of HCl
Explain why borazine is more reactive than benzene toward the addition of HCl
Why are alkenes more easily oxidizedthank alkynes?
Why are alkenes more easily oxidizedthank alkynes?
In contrast to the internal alkenes being more stable in the trans configuration, cyclohexene occurs as...
In contrast to the internal alkenes being more stable in the trans configuration, cyclohexene occurs as the cis cycloalkane rather than the trans isomer. Explain why
explain hydrogen bonding as it relates to dissolving a solute in a liquid. please use more...
explain hydrogen bonding as it relates to dissolving a solute in a liquid. please use more than 100 words.
Why is free radical halogenation of alkanes using fluorine not performed? (Explain in 5 words or...
Why is free radical halogenation of alkanes using fluorine not performed? (Explain in 5 words or less.) (Fluorine Chemistry in Pharmaceuticals)
explain in terms of bonding how the presence of o2 an ozone in the ozone layer...
explain in terms of bonding how the presence of o2 an ozone in the ozone layer helps to prevent both higher and lower energy uv light from reaching the surface of the earth
Why do the addition of gums make things more spreadable, i.e., cream cheese? (chemically) Gums such...
Why do the addition of gums make things more spreadable, i.e., cream cheese? (chemically) Gums such as locust bean or xanthan.
Determine if the following statements are true or false. _____(13)_____Conjugated dienes react more quickly than isolated...
Determine if the following statements are true or false. _____(13)_____Conjugated dienes react more quickly than isolated alkenes and can be reacted with selectively. _____(14)_____ The thermodynamic product is the fastest formed product. _____(15)_____The thermodynamic product and kinetic product are always different products for all reaction types. _____(16)_____ Conjugated pi systems still follow Markovnikov's rule so as to form the most stable intermediate cation. _____(17)_____Extended pi systems become increasingly reactive with electrophiles as the energy of the intermediate lowers. _____(18)_____Extended pi...
Explain the terms haploid, diploid, and polyploid. Why is polyploidy so much more common in plants...
Explain the terms haploid, diploid, and polyploid. Why is polyploidy so much more common in plants than in animals? Give examples of polyploid animals. Polyploid plants may occur naturally or they may be created intentionally by agricultural scientists. List four examples of polyploid commercial crops and explain why they are superior to their diploid ancestors.
Aldehydes are more reactive than ketones in nucleophilic addition primarily because: A. The C=O group is...
Aldehydes are more reactive than ketones in nucleophilic addition primarily because: A. The C=O group is planar in ketones and not in aldehydes. B. The C=O group is planar in aldehydes and not in ketones. C. Aldehydes are less sterically hindered than ketones. D. Ketones are less sterically hindered than aldehydes.