Synthesize 1-phenyl-1-propanone from ethylbenzene. No mechanism required just reagents needed.
Synthesize 1-phenyl-1-propanone from ethylbenzene. No mechanism required just reagents needed.
Starting with benzene, synthesize 1-phenyl-1-butyne. Show intermediates and reagents.
Give a mechanism and a set of reagents that can be used to synthesize each of the following: a) synthesize 1-pentyne through the elimination of a dihalide b) synthesize cis-2-pentene from an addition reaction c) synthesize trans-2-pentene from an addition reaction d) synthesize a ketone from an addition reaction e) synthesize and aldehyde from an addition reaction
2) Starting from benzene, use the reagents below to synthesize acetophenone (methyl phenyl ketone). There are two possible ways to accomplish this; give both. You may draw the intermediates in any format. Starting from benzene you have to figure out how to make the appropriate Grignard reagent 2 in two steps... 3) A, B, C, D, E? Route A: Choose one СН3 Na2Cr207 H.S04. H2O H30® workup Now convert Intermediate 2 to acetophenone... 2- acetophenone Route B: Choose one 3)...
show the reactants and reagents that would be needed to synthesize this compound from an ether ОН
_________________________________________________________________________________________________________________________________ d. Prepare octane from 1-pentyne, indicate each needed reagents. e. Synthesize cis-2-hexene from 1-pentyne and an alkyl halide. f. Synthesize trans-2-hexene from 1-pentyne and an alkyl halide. Synthesize each compound from acetylene. You may use any other organic or inorganic reagents. a.
just provide the missing reagents. No mechanism needed. H3CO PO OTS BY BY В. Ви
Synthesize this from 4 carbon or less alcohols and any organic or inorganic reagents needed and any inorganic compounds. Include all mechanisms, steps, reagents, and reactions used. СН3 NH2 СН3
Synthesize this from 4 carbon or less alcohols and any organic or inorganic reagents needed and any inorganic compounds. Include all mechanisms, steps, reagents, and reactions used. CH3 NH2 СН3
Q.2 Describe how IR carbonyl and specific other absorbances can distinguish propiophenone from 1-phenyl-2-propanone and p-ethylbenzaldehyde.