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How did it go?....I found the paper lengthy, too many suggestions...Apps weere easy except Q7...
What GT u think ?
What GT u think ?
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was so bad,...................wt about second que it was so irritating....How did it go?....I found the paper lengthy, too many suggestions...Apps weere easy except Q7...
What GT u think ?
can anyone start chat,,,.........................I found the paper was not difficult but tricky, esp the polymer quest, and entalphy.
Some repetition in section b
it was not that difficult man, enthalpy required critical approach..as for NMR some good luck but u can never be sure abt suggestions, excluding all these parts, yeas the paper was relatively easier..I thought it was ridiculously easy.
Can you stop repeating yourselfI found the paper was not difficult but tricky, esp the polymer quest, and entalphy.
Some repetition in section b
Did anyone get 0.0560 or something as the concentration of A in the electrochemistry/organic henna question?
also, what was used to reduce that compound? A strong reducing agent like LiALH4 right? because NaBH4 is too weak Im assuming
NO PAPER DISCUSSIONDid anyone get 0.0560 or something as the concentration of A in the electrochemistry/organic henna question?
also, what was used to reduce that compound? A strong reducing agent like LiALH4 right? because NaBH4 is too weak Im assuming
not the carboxylic acid man ....that was the trrick .....it must ahave been acyl chloride....cos phenold doesnt reacts with carboxylic acid.....and come on chat leave discussion here....cum onj CHAT GUYXAnd for the polymer question, the monomers were a Dicarboxylic acid and a Dihydric Phenol right? (Phenol with 2 OH groups) and the modification would be to use instead of the phenol, a Di phenyl amine, so that Hydrogen bonds can form between amide chains ( Just like in secondary stucture of proteins)
And the conditions was NaOHaq and The Dihydric Phenol ( To produce the phenoxide ion) Heat under reflux with Conc H2So4, to remove the H2O
Somebody got tricked ..not the carboxylic acid man ....that was the trrick .....it must ahave been acyl chloride....cos phenold doesnt reacts with carboxylic acid.....and come on chat leave discussion here....cum onj CHAT GUYX
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