hi there, i have a compund wihch p tert-butyl side chAIN OF CARBOYLIC ACID ATTACHED TO ANILINE ON THE OTHER SIDE.

THE TERT BUTYL SIDE CHAIN INTERGRATION IS OFF.

CAN ON EXDPLAIN THIS , TLC , NMR OF THE INTERMEDIATE CONATIN TERT BUTYLSIDE CHAIN OF BENZOIC ACID IS CHARACTERIZED WEL AND THE AMIDE BOND FORMED, WHEN MAKING ETHER ON THE OTHER SIDE ON THE COMPOUND THE TERT BUTY DISAPPEARD, THE PROCEDUCR FOR ETHER IS MITSUNOBU REACTION .

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