Explain : Benzimidazole is also known as 1,3-benzodiazoles the. The NH group present in benzimidazole is relatively strongly acidic and also * .weakly basic
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Q: c) A tertiary (1°) ammonium salt with molecular formula C6H16NBr
A: Many structures are possible C6H16NBr
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Q: i) CH3CH2COH ii) F3CCOH ii) CI3CCH,COH
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Q: the structures of cocaine (right) and its free base (l
A: The structures of cocaine (right) and its free base (left) is represented as follows:
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Q: Which of the two compounds shown below is acidic? Why
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Q: n benzimidazole How NH group behaves as acidic and basic?
A: The given molecule is: benzimidazole. How NH group behaves as acidic and basic?
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Q: -NH2
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Q: Given the structures of cocaine (right) and its free base (left) below: a. Would you expect K for…
A: The structures of cocaine (right) and its free base (left) is represented as follows:
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- Which of the ff statements is false? In aqueous solution the order of base strength R3N > R2NH > RNH2 > NH3. Alkyl groups increase the electron density on nitrogen, making the amine more basic. Alkyl groups stabilize the positive charge on the conjugate acid making the ammonium ion less acidic. Solvation through H-bonding with water is more important in the conjugate acid than in the free amine.Show how acid derivatives hydrolyze to carboxylic acids under either acidic or basicconditions. Explain why some acid derivatives (amides, for example) require muchstronger conditions for hydrolysis than other derivatives.Rank the following in order of acidity with 1 being the most acidic
- __________ will exist as a racemic mix. Chloro ethyl methyl amine Phenyl amine Ammonia Methyl diphenyl propyl ammonium chloride Diethyl amine Thank you!H3C-O-SiH3 ether, which is similar to dimethyleters, was synthesized. This ether is known to be a weaker base than (CH3)3O. Discuss why and explainRank the following compounds in order of their acidity.