Generally Carbonyl Compounds undergo Nucleophilic addition reaction.
Aldehyde is more reactive towards nucleophile than Ketone since it has only one alkyl group while in the case of ketone there are two alkyl groups which decreases the electrophilicity of carbonyl carbon by donating the Electron. Hence ketone is less reactive towards nucleophile.
More the alkyl group (size) ,less le the reactivity of Ketone and Aldehyde. Because of this reason, farmaldehyde is the most reactive carbonyl compound.
Hence order
C < D < A < E < B
2. Reactivity of Aldehydes and Ketones a. Rank the following aldehydes and ketones in order from...
Please explain using Aldehydes and Ketones terms! Chem 202, Autumn 2019 Homework Packet 10 (Aldehydes and Ketones) 2. Reactivity of Aldehydes and Ketones a. Rank the following aldehydes and ketones in order from LEAST reactive to MOST reactive: H Н Н Н А В b. Justify your answer thoroughly in words: ш
20) Rank the following Carboxyllic Acid derivatives in decreasing order (Most to Least) of reactivity towards Nucleophillic Substitution reactions? 3 Pts "NH2 II III IV More Reactive: Least Reactive 21) Match the following? 2 Pts 1) Alkynes 2) Aromatic Compounds 3) Aldehydes/Ketones 4) Carboxyllic acid derivatives A) Nucleophillic Addition Reactions B) Nucleophillic Substitution Reactions C) Electrophillic Additon Reactions D) Electrophillic Substitution Reactions
1. Rank the following carbonyl compounds from 1 to 5 in order of decreasing reactivity towards nucleophilic attack (i.e., from 1 for most to 5 for least reactive). Н Н. OCH I CH3 NO2 CHE CH3 NO2 CH3
Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reactions (most to least reactive from left to right in the answer) yucuruit pun Rank the following compounds in order of decreasing reactivity in a nucleophilic acyl substitution reaction (most to least reactive from left to right in the answer): ei ole C>A>D>B A>C>D>B A>C>B>D C>A>B>D
2. Rank the following carbocations in order from least stable to most stable THEN justify your answer thoroughly in words A B C D
Part A Rank the following carboxylic acid derivatives in order of decreasing reactivity. Rank from most to least reactive. To rank Items as equivalent, overlap them Reset Help walio ΝΗ: Most reactive Least reactive Submit Request Answer 2 A 31 If you wanted to directly synthesize the following molecule: NH which of these acid chloride derivatives could you potentially use as a starting material without converting it to another derivative first? Check all that apply. Submit Request Answer Provide Feedback
Consider the following aldehydes and ketones. Which is the correct ranking in order of increasing reactivity towards nucleophilic addition to the carbonyl group? A) 2-methylcyclohexanone < cyclohexanone < CH3CHO < H2CO B) CH3CHO < 2-methylcyclohexanone < cyclohexanone < H2CO C) cyclohexanone < 2-methylcyclohexanone < H2CO < CH3CHO D) H2CO < cyclohexanone < CH3CHO < 2-methylcyclohexanone E) cyclohexanone < 2-methylcyclohexanone < CH3CHO < H2CO
Rank the following compounds in order of increasing reactivity towards nucleophilic attack. Be sure to answer all parts. A) B) C) CA Least Reactive Most Reactive
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution. Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive Least reactive butyl acetate benzoic anhydride 3-methylpentanoyl chloride propionamide
H 7. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the most reactive compound as compound 1 and the least reactive compound as compound 5. (5 points) NO2 pada CH SO3H OH 5