WebReaction of CH 3 CONH 2 as a base. In the case of CH 3 CONH 2, the electron pair is delocalized by resonance. This makes them less available for electron donation. Hence … WebThe compunds X and Y are respectively. Class 12. >> Chemistry. >> Amines. >> Preparation of Amines. >> The compunds X and Y are respectively. Question. OR a) …
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Web1) Applying resonance. Amides such as acetamide (CH3CONH2) are much weaker bases than amines, such as ethylamine (CH3CH2NH2). Explain why (try resonance). Predict also how protonation (reaction with H+) of both species would go (again, resonance can help). 2) Drawing Isomers based on given formula. Draw Lewis structures for: a. WebOct 1, 2024 · Due to reduction in electron density on N – atom of CH 3 CONH 2, it is a weaker base than CH 3 CH 2 NH 2 chihuly missouri botanical garden
Acetamide CH3CONH2 - PubChem
WebJul 9, 2024 · Explain.4) How can tri-substitution by bromine be prevented in aniline?5) How can we prepare mono bromoaniline from aniline?6) Give reasons -a) (CH3)2NH is more basic than (CH3)3N in an aqueous solution.b) Acetylation of – NH2 group is done in aniline before preparing its ortho and para compounds.c) Aliphatic amines are stronger bases … WebThe compunds X and Y are respectively. Class 12. >> Chemistry. >> Amines. >> Preparation of Amines. >> The compunds X and Y are respectively. Question. OR a) CH3CONH2 is a weaker base than CH3CH2NH2. Why? li. WebExplain why CH3CONH2 is a stronger acid and a weaker base than CH3CH2NH2. Expert's Answer Solution.pdf Next Previous Related Questions Q: The explanation for this problem is that the inductive and electronegative effects in the conjugate. 12. ?. Acidity of Melamine NHs is greater than acidity of aniline NH, since the stability of conjugate... chihuly montreal