Examples of 'carbocation' in a sentence
Meaning of "carbocation"
Carbocation: An organic ion that contains a positively charged carbon atom
Show more definitions
- any cation containing an excess positive charge on one or more carbon atoms
How to use "carbocation" in a sentence
Basic
Advanced
carbocation
The formation of a carbocation from a halogenoalkane is an example of.
We have given away an electron to this carbocation.
The resulting carbocation is then attacked by a molecule of water.
These experiments revealed the carbocation to be fluxional.
The order of carbocation stability is tertiary secondary primary.
The alpha carbon is the carbocation carbon.
The carbocation initiates the polymerization.
It occurs to form an even more stable carbocation.
The remaining tertiary carbocation is quenched by a molecule of water.
The water molecule is lost to produce a carbocation.
This step provides a carbocation as an intermediate.
It will donate an electron to this carbocation.
This intermediate carbocation can rearrange.
It is giving away an electron to the carbocation.
Stabilization of the carbocation intermediate lowers the activation energy.
See also
This reaction involves the formation of a carbocation intermediate.
A carbocation is one which carries a positive charge on a carbon atom.
The mechanism involves carbocation intermediates.
The carbocation is now neutral.
One being the formation of a carbocation intermediate.
Corannulene can react with electrophiles to form a corannulene carbocation.
This reaction involves a carbocation rearrangement.
Now this magenta electron has been donated to the carbocation.
Carbocation rearrangements are more common than the carbanion or radical counterparts.
So this electron could be given to this carbocation right there.
The carbocation had a positive charge because it had lost it originally.
You have a tertiary carbocation.
The most stable carbocation will produce the fastest reaction.
It can actually be a stable carbocation.
A carbocation intermediate is formed.
This leads to formation of a carbocation.
This is known as a carbocation since the positive charge is on a carbon atom.
So alkyl groups help to stabilize the positive charge on a carbocation.
The resonating bond is broken and a carbocation resonating structure results.
The halogen is now the nucleophile recombining with the carbocation.
There forms a polysulfide of ammonium and carbocation as revealed by the elementary analysis.
Both of them can carry out the nucleophilic attack on the carbocation.
He is now a carbocation.
The alcohols are not otherwise purified as the following reaction takes place by carbocation.
Remember that carbocations can rearrange the molecule to form the most stable carbocation.
Deprotonation of the carbocation.
The resonance stabilized BG carbocation mass code yields an intense signal with LDI mass spectrometry.
The formation of a carbocation.
Subsequently, the carbocation is reduced by a hydrogen donating agent.
Mechanistic investigations support the formation of a carbocation in the catalytic cycle.
Carbocation rearrangement reactions occur through three-center bond transition states.
The activation temperature decreases if a more stabilized carbocation can be formed.
Nucleophilic attack, the carbocation reacts with the nucleophile.
The reaction proceeds via protonation to give the more stable carbocation intermediate.
A carbocation may be stabilized by resonance by a carbon-carbon double bond next to the ionized carbon.
