CHAPTER 26- CARBOXYLIC ACIDS AND THEIR DERIVATIVES 🤎 Flashcards
Using an equation and necessary diagrams, explain the acidity of carboxylic acids
-Compare the relative acidities of carboxylic acids to that of alcohols and phenols
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Using an equation and necessary diagrams, explain the relative acidity of chlorine-substituted carboxylic acids in detail
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State which two carboxylic acids an get oxidised
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Write out the equation for the oxidation of methanoic acid, list the colour changes of the oxidising agents
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Write out the equation for the oxidation of ethanedioic acid, list the colour changes of the oxidising agents, state any observations made
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Describe the structure of an acyl chloride
-Compare the reactivity of an acyl chloride to that of a carboxylic acid
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Write equations for the reactions between a carboxylic acid and three reagents to produce the corresponding acyl chloride
-State any observations made or requirements for these three reactions
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Explain why acyl chlorides are less/more reactive than carboxylic acids
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Write a general reaction and draw a mechanism for the hydrolysis of acyl chlorides
-Explain IN DETAIL what occurs at each stage of this reaction
-State the conditions of this reaction
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Write a general reaction and draw a mechanism for reaction of an acyl chloride with an alcohol
-Explain IN DETAIL what occurs at each stage of this reaction
-State the conditions of this reaction
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Write a general reaction and draw a mechanism for reaction of an acyl chloride with phenol
-Explain IN DETAIL what occurs at each stage of this reaction
-State the conditions of this reaction
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Write a general reaction and draw a mechanism for reaction of an acyl chloride with ammonia
-Explain IN DETAIL what occurs at each stage of this reaction
-State the conditions of this reaction
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Write a general reaction and draw a mechanism for reaction of an acyl chloride with a primary amine AND a secondary amine
-Explain IN DETAIL what occurs at each stage of this reaction
-State the conditions of this reaction
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Draw an example of an acyl chloride, alkyl chloride and a halogenoarene
-State which is the most difficult and least difficult to hydrolyse and explain why
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