basicity and nucleophilicity has some difference dude !...
thats why they have two different names !
good work though subash !! :)
did u get btw how is it determined ?
"nucleophilicity runs parallel to basicity when the nucleophilic atom is the same in various species"
basicity and nucleophilicity has some difference dude !...
thats why they have two different names !
good work though subash !! :)
did u get btw how is it determined ?
subash but that just simply implies that OH- is more BASIC than HS-
its not neccessary that it is the same in the case of nucleophilicity !
after all they are two different terms :D
hmm ...ultimately compare theIR electronegativity then ! :D
so by comparing H2O is a weaker acid than H2S
so OH- would be the stronger base and hence nucleophile
am i rite
subash no yaar !! ..its not ! ..its the other way round!
coz u know ...just compare the conjugate of h2o and h2s
@ unique did u say that to me or what
asking because ur reply had same timing as mine
i think i just saw this question H2O is more stable than H2S so OH- would obviously be the better nucleophile
becaz OH- bond is tough to break than HS- moreover O is more electronegative than Sulphur am i rite unique
and prajith ?.. u did not get my question correctly ?..,what are u doing with bonds here ?... throw them away !! .. n think the other way !
ok sankara and in ur amine question .. u are ,missing a catalyst ..otherwise reduction of that amino compound would give only aniline !
UNIQUE I HAVE MY REVISION EXAMS TOMORROW.I HAVE TO GET UP EARLY AND I HAVE TO COMPLETE MY TODAYS WORK CAN I JOIN IN THIS DISCUSSION TOMORRROW
UNIQUE CAN U GIVE ME SOME RELATION ABT ELECTRONEGATIVE OF THE SULPHUR AND OXYGEN
I AM ALSO WEAK IN MECHANICS ESPECIALLY IN ROT MECHANICS
CAN U CREATE A DISCUSSION ON THAT CHAPTER ALSO
the timing of mine and sankara post is same...so it struck in our mind at the same time....
@srinath ...you said weaker bases make better nucleophiles. Can you give an example? As far as I understand weaker base has better leaving ability...
a small teaser here : quiniclidine and triethylamine are excellent bases (known from pka values)...so can they be excellent nucleophiles too....discuss separately for both compounds !!
comparing the e.c of the ions and their atoms should give you the answer.
out of the following ions,
identify the least stable ion !
Li-, Be-, B- , C- ??
WITH REASON !!