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Card 26
Front
The primary reason why some amino acids have acidic/basic groups which are more/less basic than others
Back
Card 27
Front
The name given to the pH at which a zwitterion carries no net charge
Back
Card 28
Front
The name of the type of amino acid synthesis in which the reagents are an aldehyde, NH3 and HCN
Back
Card 29
Front
The reagents needed for the hydrolysis stage in Strecker synthesis of amino acids
Back
Card 30
Front
The substance required to react with a carboxylic acid in order to produce an acyl chloride
Back
Card 31
Front
A common example of a carbodiimide activates carboxylic acids in situ
Back
Card 32
Front
This protecting group can be removed by reacting with HBr in acetic acid
Back
Card 33
Front
This protecting group can be removed by reacting with HCl or CF3COOH in acetic acid
Back
Card 34
Front
This protecting group can be removed by reacting with piperidine
Back
Card 35
Front
The molecule involved in automated peptide synthesis
Back
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