decarboxylation

decarboxylation can occur in the following class of compounds:

(1)β-keto esters

(2)1,1 dicarboxylic acids( generally called "LAMNAC" rule)

(3)β,γ unsaturated acids

additional note: decarbonylation (-CO) occurs in the case of α-keto esters or α-keto acids.

where are they ?

okay .. i will try them for sure :)

even i support u plz try out my other doubts

i dunno ... but i am quite sure abt my explanation ...

bansal sheet question

this is from which book ... ??

i dunno... ans may be wrong ...

Which type of decarboxylation: Soda lime or the other one (involving electrolysis....i don't remember it's name)?

Cos the latter occurs via free radicle formation.....whose stability can differ with the halogen group attached.

dont say this mathie..................[2]
yesterday only u were solving chem problems in such a gr8888 way......[5]

but -i effect of f is more than cl how would u justify that

rate in second will be more...

since electronegativity of F is more than Cl.

so the carbanion formed is more stabilised in second one...

anywys i am not gud at chemistry...... leave it...............

ur ans is right but not explaination if f is more electronegative than charge is more dispersed n thus more stable

if thats the case eureka, then obviously first one will b e more stable as chlorine is less elctronegative than flourine.

soda lime