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Addition

-Harvard unervisty

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Q: What is faster substitution or addition reactions?
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What has the author Gary Craig Hanson written?

Gary Craig Hanson has written: 'Mechanistic study of some internal substitution reactions and a substitution at sulfenyl sulfur' -- subject(s): Substitution reactions


What r products of chlorine and humic acid reaction?

Chlorinated products of humic acid (or polyphenols) are formed (by substitution and or addition reactions) which gives them an awefull odor.


What has the author Keith U Ingold written?

Keith U. Ingold has written: 'Free-radical substitution reactions' -- subject(s): Substitution reactions, Radicals (Chemistry)


What are substitution reactions of Alkane?

Yes, it can be converted thermally or photochemically by dehydrogenation using iridium complexes as catalysts.


How do you write the nucleophilic substitution reactions for aniline and toluene?

aniline would go through an electrophilic substitution, it is a weak base


Is esterfication a substitution or addition reaction?

It is substitution because hydrogen of carboxylic acid is replaced by an alkyl group.


Why butane undergoes substitution reactions?

due to saturated and single bonded.


What is the use of acetylides formation?

Acetylide formations are very useful inorganic chemistry reactions in combining carbon chains, particularly addition and substitution reactions.


Chemical reactions in cells are faster than the same reactions outside cells?

Chemical reactions in cells are faster than the same reactions outside cells.


What type of reaction is exhibited by alkenes?

Alkynes undergo many addition reactions such as: catalytic hydrogenation, addition by electrophilic reagents, hydration with tautomerism, hydroboration reactions, and oxidations. They also undergo nucleophilic addition reactions & reduction. Finally alkynes are the strongest bronsted acids made from only hydrocarbons.


Why benzene undergoes electrophilic substitution reaction whereas alkenes undergoes addition reaction?

The cation formed upon addition of an electrophile to benzene is highly stabilized by resonance,whereas the cation formed to an alkene is stabilized by hyperconjugation. The loss of a proton in benzene is favourable due to the restoration of the cyclic pi-system.


Why phenol undergoes electrophillic substitution reactions?

because, phenol it self neucleophilic group.