QUESTION 8 Too much acid added during neutralization could lead to the formation of dehydration products. Which structure is a reasonable dehydration product of hydrobenzoin? APHICH Ph OB. Ph-CH2-CH2-Ph OC. Ph-CO-CH2-Ph O D. Ph-CH=CH Ph

Draw the product formed when phenylacetic acid (C6H5CH2COOH) is treated with each reagent. With some reagents, no reaction occurs. a. NaHCO3 b. NaOH c. SOCl2 d. NaCl e. NH3(1equiv) f. NH3, ∆ g. CH3OH, H2SO4 h. CH3OH, −OH i. [1] NaOH; [2] CH3COCl j. CH3NH2, DCC k. [1] SOCl2; [2] CH3CH2CH2NH2 (excess) l. [1] SOCl2; [2] (CH3)2; [2] (CH

MONTR Cryahoga Commnity College 27) Hydrolysis of an ester: O II CH,-C-O-CH,-CH,-CH,+ H,O 28) Acid/ Base reaction of an amine CH3-CH2-NH, + H2CO3 29) Hydrolysis of an amide O II CH3-CH2-CH2-CH2-CH2-C-NH-CH2-CH2-CH, + H20

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