Amino Acids, Amides And Chirality Flashcards

1
Q

What are α-amino acids? And what’s there general formula?

A

Organic molecules containing a carboxylic acid group and an amine group bonded to the same carbon atom. Their general formula is RCH(NH2)COOH

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2
Q

What do the two functional groups within a single molecule mean about amino acids?

A

Can behave as both an acid and a base, depending on the conditions of the reaction

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3
Q

What would the carboxylic acid group do?

A

Will react with alkalis and donate a proton.

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4
Q

What would the amine group do?

A

Amine group is basic and will react with acids to accept a proton

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5
Q

What are zwitterions?

A

diplomat with a positive charge in one part of the molecule and a negative charge in another part of the molecule. So amine group is positive and carboxyl group is negative.

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6
Q

Draw a primary amide

A

Check pmt q

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7
Q

What groups do amides contain?

A

A C=O group and NHR group where R is an alkyl group or a hydrogen atom. They have the structure RCONH2.

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8
Q

Draw a secondary amide (N-substituted amide)

A

They have an additional carbon chain bonded to the nitrogen atom.
Check pmt

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9
Q

What reaction can amines undergo?

A

Nucleophilic addition-elimination reactions with acyl chlorides to produce amide and N-substituted amides.

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10
Q

What is chiral centre?

A

A carbon atom with four different groups bonded around it, so that the molecules has no line of symmetry. Commonly indicated with a ‘*’.

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11
Q

Define optical isomerism and an optical isomer

A

A type of stereoisomerism where molecules have the same molecular formula but a different spatial arrangement of atoms.
The presence of a chiral centre leases to two possible isomers that are non-superimposable mirror images of each other. These are called optical isomers.

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