Select ALL the functional groups found in aspirin:Group of answer choicesketonealdehydecarboxylic acidamideesteralcoholamine
Question
Select ALL the functional groups found in aspirin:
- ketone
- aldehyde
- carboxylic acid
- amide
- ester
- alcohol
- amine
Solution
To determine the functional groups present in aspirin (acetylsalicylic acid), let’s identify the components of its molecular structure.
Step 1: Identify the Structure of Aspirin
Aspirin has the chemical formula C₉H₈O₄. Its structure consists of:
- An acetyl group (-COCH₃)
- A salicylate group, which includes a carboxylic acid (-COOH) and a phenolic hydroxyl group (-OH).
Step 2: Analyze Functional Groups
- Carboxylic Acid: Aspirin contains a carboxylic acid group (-COOH).
- Ester: The acetyl group bonded to the salicylate structure forms an ester bond.
- Alcohol: The phenolic -OH group qualifies as an alcohol functional group.
- No Ketone or Aldehyde: The molecule does not contain a ketone (R-CO-R') or aldehyde (R-CHO) functional group.
- No Amide or Amine: Aspirin does not have an amide (R-CONH₂) or amine (R-NH₂) functional group.
Step 3: Confirm Findings
The functional groups can be summarized as follows:
- Carboxylic Acid: Yes
- Ester: Yes
- Alcohol: Yes
- Ketone: No
- Aldehyde: No
- Amide: No
- Amine: No
Final Answer
The functional groups found in aspirin are:
- Carboxylic acid
- Ester
- Alcohol
Similar Questions
Select ALL the functional groups found in aspirin:Group of answer choicesketonealdehydecarboxylic acidamideesteralcoholamine
Aspirin is known as :acetyl salicylic acidphenyl salicylateacetyl salicylatemethyl salicylic acid
Consider the molecule above. What is the name of the functional group labelled B?Group of answer choices
CH3-CH2-NH-CH3Name the compound aboveGroup of answer choicesEthylaminemethylamineEthylmethylaminepropylamine
Which functional group is NOT found in penicillin? A.AmideB.ImineC.Carboxylic acidD.Thioether
Upgrade your grade with Knowee
Get personalized homework help. Review tough concepts in more detail, or go deeper into your topic by exploring other relevant questions.