No i think oxidant is the substance that get oxidized......r u sure about ur statement?yes of course it is
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No i think oxidant is the substance that get oxidized......r u sure about ur statement?yes of course it is
no oxidants are oxidising agents !!! Seriously
I think its decreased ! Correct me if wrong
Thankyou bothIf the volume is increased, concentration must decrease and therefore rate will decrease.
I guess
volume and concentration are inversely proportional!!Thankyou both
i think it can. dunt know...STATE WHY THIS CAN NOT GIVE A CARBOXYLIC ACID IN PRODUCT WHILE OTHER ISOMER OF IT CAN GIVE IT ..!!?? AND WHAT ITS NAME MEANS PROPANOL-2-OL ..!!!
View attachment 10441
alcohol's functional group is OH not O-H , there is no bond between O and H , thats whats wrongSTATE WHY THIS CAN NOT GIVE A CARBOXYLIC ACID IN PRODUCT WHILE OTHER ISOMER OF IT CAN GIVE IT ..!!?? AND WHAT ITS NAME MEANS PROPANOL-2-OL ..!!!
View attachment 10441
THNX FOR THE NAMEi think it can. dunt know...
the name means that the OH group is linked to the second carbon
alcohol's functional group is OH not O-H , there is no bond between O and H , thats whats wrong
STATE WHY THIS CAN NOT GIVE A CARBOXYLIC ACID IN PRODUCT WHILE OTHER ISOMER OF IT CAN GIVE IT ..!!?? AND WHAT ITS NAME MEANS PROPANOL-2-OL ..!!!
View attachment 10441
Year please !THNX FOR THE NAME
BUT IN PASTPAER ATP A QUESTION CAME
Q) a student found that different alcohol,altough having the same formula did not give a carboxylic acid as the product,suggest the name and structure of this alcohol
name.....................................
structure __________________________
so i posted its answer asking its reasons ..!! pls confirm me soon
The OH should be on the side of the structure i guess.
That's the same thingalcohol's functional group is OH not O-H , there is no bond between O and H , thats whats wrong
Year please !
That's my answer lol, in this isomer, OH is in the middle, so maybe its more stable like this. Besides, the carboxyl group is always on the end of the structure so it can not be oxidised! MY GUESS.dats what the difference in isomers but why cant it can produce carboxylic ????????????????/ thats the real confusion !!!!!!!!!!
That's my answer lol, in this isomer, OH is in the middle, so maybe its more stable like this. Besides, the carboxyl group is always on the end of the structure so it can not be oxidised! MY GUESS.
THNX FOR THE NAME
BUT IN PASTPAER ATP A QUESTION CAME
Q) a student found that different alcohol,altough having the same formula did not give a carboxylic acid as the product,suggest the name and structure of this alcohol
name.....................................
structure __________________________
so i posted its answer asking its reasons ..!! pls confirm me soon
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