Naming Carboxylic Acid Derivatives
Topic Page
Naming Carboxylic Acid DerivativesQuestions
- How are carboxylic acid derivatives named?
- What steps are used to name primary amides?
- What is the common name of the solution of acetic acid and water?
- What is the structural formula for zinc benzoate?
- What is the structural formula of calcium propanoate?
- What steps are used to name secondary and tertiary amides?
- According to IUPAC, what is the name of #(CH_3CH_2)_3C# #COOH#?
- What is the structural formula for sodium hexanoate?
- What are the structural formulas for cyclohexyl propanoate and methyl formate?
- How can I draw the structures of 4 isomers of amides for the formula #C_5H_11NO# ?
- What is the difference between an ether and an ester?
- Which substances have both a carboxylic acid functional group and an alcohol functional group?
- Question #d89a9
- Question #5fa25
- Question #6fe80
- How many carboxylic acids have the formula C4H8O2?
- What is formed when carboxylic acids react with metals and metal carbonates?
- What do deamination and decarboxylation reactions have in common?
- How many times does decarboxylation occur in the aerobic breakdown of one glucose molecule and when does it occur?
- What is the chemical equation for the decarboxylation of butyric acid with soda lime?
- How can niacin be decarboxylated to pyridine?
- Why is the ornithine decarboxylation reaction indicated by a purple color and a negative is yellow?
- What is the product of the thermal decarboxylation of dimethylpropanedioic acid?
- What is the product of the thermal decarboxylation of dimethylpropanedioic acid (dimethylmalonic acid)?
- What is the product of the decarboxylation of trytophan?
- Question #268a8
- Question #c1767