Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (somy):
these are the questions
OpenStudy (somy):
in question 21 i do understand why its B but i do not understand why its not A or C or D
OpenStudy (somy):
in question 24 i do understand that attacking group is nucleophile, but why leaving group is also nucleophile?
OpenStudy (somy):
@Abhisar here u go
OpenStudy (abhisar):
hmmm..looks like i can do this
Still Need Help?
Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (abhisar):
ohkay..for question no 21, do u agree NH3 is a nucleophile ?
OpenStudy (abhisar):
????
OpenStudy (somy):
mmmm yes because it has a lone pair
OpenStudy (abhisar):
yep.. ur correct..so now do u agree that C is wrong ?
OpenStudy (abhisar):
because the question says ALWAYS applies
Still Need Help?
Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (somy):
ohw yeah right
OpenStudy (somy):
how about A and D?
OpenStudy (somy):
@KL-RC here
OpenStudy (abhisar):
NH3 is not negatively charged. Is it ?
OpenStudy (somy):
owh yeah its not
Still Need Help?
Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (somy):
is it neutral?
OpenStudy (anonymous):
I think it should be neutral too
OpenStudy (abhisar):
yes it is neutral...it has a lone pair
OpenStudy (somy):
yeah yeah
OpenStudy (somy):
so D is rejected
Still Need Help?
Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (abhisar):
yep
OpenStudy (somy):
okaaaay now A
OpenStudy (abhisar):
nucleophiles react at the sites which are e deficient. ryt ?
OpenStudy (anonymous):
yes!
OpenStudy (somy):
oh wait i got it nucleophile can attack a functional group of halogen alkanes!!! and its single bond, and its nucleophilic substitution!!!
Still Need Help?
Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (abhisar):
\(\color{green}{\text{Bingo !!}}\)
OpenStudy (anonymous):
Oooooohhh ok!
OpenStudy (somy):
yaaaay! :D clear now!! thxn!! @Abhisar
how about next question?
OpenStudy (abhisar):
That's the point i said..i dont remember organic reactions any more...i studied them long time ago..!!
:(
OpenStudy (somy):
owhhhhhh
Still Need Help?
Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (anonymous):
awww daim!
lol
OpenStudy (somy):
i got it myself lmao
OpenStudy (abhisar):
LOL...even i got it !!
OpenStudy (abhisar):
u still want me to xplain ?
OpenStudy (somy):
lmao ahahah cool share it i'll share too
Still Need Help?
Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (abhisar):
ohkay....!!
OpenStudy (abhisar):
well this reaction is a NUCLEOPHILIC substitution reaction. The bromine of the bromoalkane is substituted by the alcohol and the bromine is liberated
OpenStudy (somy):
bromoethane is hydrolysed
the product of hydrolysis will be ethanol and Br-
OH- is attacking and its nucleophile
Br as it starts breaking from Carbon
carbon will have partial positive charge and Br partial negative charge
Br has is negatively charge that means it has extra electron meaning it can donate it thus it is also nuclephile
OpenStudy (abhisar):
yes here u go !!
OpenStudy (abhisar):
Still Need Help?
Join the QuestionCove community and study together with friends!
Sign Up
OpenStudy (somy):
lol i messed up in the end explanation but i hope u get it lol i was too fast
OpenStudy (abhisar):
yeahhh..check the reaction
OpenStudy (abhisar):
so u can see both OH and Br are nucleophiles
OpenStudy (somy):
yesss lol cleared it myself lmao
OpenStudy (anonymous):
thanks @Somy @Abhisar
Still Need Help?
Join the QuestionCove community and study together with friends!