1. Reactivity of-
Acid Chloride > Acetic anhydride > Methyl Acetate > Acetic acid > Methyl acetamide
2. More negative Gibbs free energy of formation means, the compound is formed more spontaneously i.e. the forward reaction is more favorable. Now reactivity means, how fast the compound is combining with other reagents or maybe participating in decomposition. Hence, as the formation of a compound and its reactivity is inversely proportional, more negative Gibbs energy of formation a compound has, more stable it would be i.e. lower will be its reactivity.
1) Rank from most to least reactive. acetic acid, methyl acetate, methyl acetamide, acetic anhydride, acetyl...
Please rank the following acid derivatives from most reactive to least reactive toward nucleophilic attacks and explain your reasoning. 1. NH2 2. Please show how you would accomplish the following synthesis. heptanoyl chloride heptanoic anhydride CI cyclopentanecarbonyl chloride 2-propyl cyclopentanecarboxylate heptanoyl chloride N-cyclohexylheptanamide OH cyclopentyl acetate cyclopentanol
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution Most reactive acetyl chloride hexyl propanoate Least reactive acetic anhydride propionamide
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most reactive acetyl chloride propionamide benzoic anhydride isopropyl benzoate acetaldehyde propanone Least reactive
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most Reactive to least reactive. 3-methylpentanoyl chloride, acetic anhydride, hexyl propanoate, N,N-diphenylethanamide, butanedial, and propanone.
4. Rank these carboxylic acid derivatives in order of least reactive to most reactive towards nucleophilic acyl substitution reactions. (4 points) i لیل OMe NH2 1 2 3 Least Most
QUESTION 1 Propanoyl chloride reacts with an acetate anion to give which product? Acetic propanoic anhydride propanoic acetic anhydride propyl acetate Cacetyl propanoate QUESTION 2 Reaction of benzoic acid with thionyl chloride produces compound A. Compound A is reacted with 2 moles of ammonia to give compound B which is then reacted with thionyl chloride to furnish compound C. Compounds C is then treated with NaOH in the first step and acidified with acid in the second step to give...
Rank according to carboxilic acid deravitive reactivity. 1 most reactive, 5 least reactive a b c d e
1. (2 point) Rank the following alkyl bromides from most reactive to least reactive in an S2 reaction. Explain your reasoning. a. 1-bromo-2methylbutane b. 1-bromo-3-methylbutane C. 2-bromo-2-methylbutane d. 1-bromopentane Most Reactive Least Reactive
the tests performed were: •hydrolysis of acid derivatives- esters, amides •alcoholysis: Schotten-Baumann reaction- acetic acetyl chloride, acetic anhydride •aminolysis:anilide formation •hydroxamic acid test uations involved in the chemical tests. it necessary ary to perform a preliminary test on the sample before doing the hydroxamic acid 2 W est: necessany to perfom a preliminary kst on the sam ple bsfore doing mic auicl test bese pylnery st eliminates the phenels ard t is the hadroxamic Unbis which give felx psive reso...
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