Rank the carbonyl-containing compounds in order of susceptibility to nucleophilic attack from most reactive to least reactive. isopropyl benzoate butanoyl chloride butanedial Most susceptible Least susceptible Answer Bank 5,5-dimethyl-3-heptanone benzoic anhydride propionamide

Draw the reaction of the Grignard reagent interacting water and the product produced. bromobenzene Br MgBr Mg ether HCI phenyl magnesium bromide (Grignard reagent) OH off triphenyl methanol

2. There are two methods to convert an alkyl halide into a carboxylic acid containing one additional carbon atom: R-X R-X NaCN CH3CI Mg R-CN Br R-MgX H3O+ 1) CO₂ 2) H3O+ (CH3)3CCI i Depending on the structure of the alkyl halide, one or both of these methods may be used. For each alkyl halide shown, write out a stepwise mechanism that converts it to a carboxylic acid. If both methods work, draw both routes. If one method cannot be used, state why it cannot. HO R OH AiOH R OH Br

can I get an explanation on how to do these? Thank you

Draw the structure(s) of the major organic product(s) of the following reaction. p-toluenesulfonic acid excess CH,CH,OH benzene

Label the reactants with either electrophile, nucleophile, base or acid.