Rate of Solvolysis

se after solvosis the charge on sulpher is - which is stablize by benzene ring by resonance

ohh cool big xplanation !
fm which boook u got dis image ?
morrison boyd kyaaaaa ?

ya sngp

bt meko woh ni pata

ya....your ans was rite but i dont think steric effect plays any role here.It's basically due to "neighbouring grp.effect"

yes..... of course.

yeah the explanation to this cud be given by the neighbouring group effect...btw mates is all this stuff really there in our syllabus??

I guess all of you have different reasonings
BUT the correct ans is B i.e I >> II > III

The explanation's coming ..........

n dude !
ter is no benxene ??
kaha pe bbenzene dikh raha hai be ??
it is cyclo hexane !!!!!!!!!

accordin 2 meh i feel answer is b cuz elimination takes place in trans way so 1 structure mein trans hai .so itna hindernce ni hoga weras last mein steric hindrnce hoga

corrct meh if m wrng

ab mere vichaar bhi sun lo ghante ki behass ke baad
the fight is b/w C and D

i think
the answer must be D

my reason C₆H₅ jo hai woh solvolysis mein hindrance daalega

benjene is non polar na and doesnt solvate easily

Solvolysis is a special type of nucleophilic substitution or elimination where the nucleophile is a solvent molecule.
For certain nucleophiles, there are specific terms for the type of solvolysis reaction.
For water, the term is hydrolysis; for alcohols, it is alcoholysis; for ammonia, it is ammonolysis.
i think its C ?
CHLORINE WILL not get easily brekoff
so as it will require solvents and other special reagents !
while 1 n 3rd r almost ~same
so........lone pair of e- on cl n as well due 2 lack of resonance it will adjust by elimination
so opti9on ONLY
C OR D
BUT FINAL I THINK SOO
C ?
is it right i just think so , pls scrap me if u know final !!111

Speaking of lesser charge density , wat abt the electrons on S^.. of PhS- ??