Flashcards on Bioinorganic Chemistry: Elements in Life

Bioinorganic Chemistry: Elements in Life - Oxidative Stress & Antioxidants

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What functional group defines carboxylic acids?

The carboxyl group (–COOH).

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Carboxylic Acids & Derivatives

103 cards

Card 1

Question: What functional group defines carboxylic acids?

Answer: The carboxyl group (–COOH).

Card 2

Question: What happens when the hydroxyl (–OH) of a carboxyl group is replaced by –OR?

Answer: An ester is formed (–COOR).

Card 3

Question: How are esters named?

Answer: Analogous to salts: name the alkyl (from alcohol) then the acid-derived part (e.g., methyl acetate, ethyl benzoate).

Card 4

Question: How are esters commonly prepared?

Answer: By esterification of carboxylic acids or from more reactive acid derivatives.

Card 5

Question: Give two natural roles or occurrences of esters.

Answer: Many esters are pleasant-smelling compounds used in flavors and fragrances; esters of higher carboxylic acids (fatty acids) form fats, cerides, and co

Card 6

Question: What is a thioester in terms of carboxylic acid derivatives? (structure hint)

Answer: A derivative where –OH is replaced by –SR (O C R SR 1 shown in content).

Card 7

Question: What are acyl halides and where do they commonly occur?

Answer: Derivatives where –OH is replaced by a halogen (e.g., –Cl); acyl halides are primarily laboratory-made products, not common in nature.

Card 8

Question: How are acid anhydrides formed from carboxylic acids?

Answer: By removing water from two carboxyl groups and connecting the acid fragments (forming RCO–O–COR).

Card 9

Question: What is the general replacement that forms an amide from a carboxylic acid?

Answer: Replacing –OH with –NH2 to give an amide (–CONH2 or derivatives).

Card 10

Question: Why are amides especially important biologically?

Answer: Proteins contain amide (peptide) bonds (–CO–NH–), making amides the most important biological amides.