Industry-relevant training in Business, Technology, and Design to help professionals and graduates upskill for real-world careers.
Fun, engaging games to boost memory, math fluency, typing speed, and English skills—perfect for learners of all ages.
Enroll to start learning
You’ve not yet enrolled in this course. Please enroll for free to listen to audio lessons, classroom podcasts and take practice test.
Listen to a student-teacher conversation explaining the topic in a relatable way.
Today we're learning about aldehydes. Aldehydes have a functional group –CHO. Can anyone tell me what that means?
I think it’s the carbonyl group at the end of the chain?
Exactly! In IUPAC nomenclature, the longest carbon chain that includes the –CHO group determines the name. We use the suffix -al. Can anyone give me an example?
Methanal is an example! That's formaldehyde, right?
Correct! Good job, Student_2. Remember, for aldehydes, the –CHO group must be part of the terminal carbon.
Now, let's talk about ketones. The main difference from aldehydes is where the carbonyl group is located. Who can describe the functional group of a ketone?
It's >C=O, but it's not at the end of the carbon chain.
That’s right, Student_3! For ketones, we use the suffix -one. Our examples include propanone, which is aceton.
How do we always know the IUPAC name?
Great question! Simply name the longest chain that includes the carbonyl carbon, then add -one at the end. Remember 'K for Ketone’ and 'O for -one' to help you remember this.
Lastly, we have carboxylic acids! Who can tell me their functional group?
Isn’t it –COOH?
Exactly! And what suffix do we use for their IUPAC name?
It’s -oic acid, right?
Perfect! As an example, ethanoic acid, which is acetic acid, is a common substance in our kitchens.
Why do carboxylic acids have such strong odors?
Good question! Their acidic nature is due to the presence of the hydroxyl group (-OH) combined with the carbonyl group (C=O). This combination establishes unique scents.
Read a summary of the section's main ideas. Choose from Basic, Medium, or Detailed.
Dive deep into the subject with an immersive audiobook experience.
Signup and Enroll to the course for listening the Audio Book
• Functional group: –CHO
• IUPAC name: Based on the longest carbon chain containing –CHO. Suffix: –al
• Example: HCHO → Methanal (Formaldehyde)
Aldehydes are organic compounds that contain a carbonyl functional group (C=O) at the end of the carbon chain. The functional group for aldehydes is represented as -CHO. When naming aldehydes using the IUPAC system, we identify the longest carbon chain that contains the -CHO group, and we use the suffix '-al' in the name. For example, HCHO is named methanal, commonly known as formaldehyde.
Think of aldehydes like a street that ends with a 'C' for carbon in its name when adding it to your address. Just like a house on Main Street has 'Main' in the street name, aldehydes have '-al' at the end when you name them because their important functional group is at the end of the chain.
Learn essential terms and foundational ideas that form the basis of the topic.
Key Concepts
Aldehydes: Organic compounds with the -CHO functional group.
Ketones: Compounds with a carbonyl group >C=O that is not terminal.
Carboxylic Acids: Compounds containing both a carbonyl and a hydroxyl group, -COOH.
IUPAC Naming: Systematic naming of organic compounds.
Functional Groups: Specific groupings responsible for molecular behavior.
See how the concepts apply in real-world scenarios to understand their practical implications.
Methanal (HCHO) represents an aldehyde example.
Propanone (CH3COCH3) is an example of a ketone.
Ethanoic acid (CH3COOH) exemplifies a carboxylic acid.
Use mnemonics, acronyms, or visual cues to help remember key information more easily.
Aldehydes are at the end, it's -CHO that they send.
Once there was a family of aldehydes living at the end of their street, with the carbonyl group always in sight and their suffix -al to keep things bright.
For ketones, remember: K is for Carbonyl that's hidden, calling it ‘-one,' that’s how it’s bidden!
Review key concepts with flashcards.
Review the Definitions for terms.
Term: Aldehyde
Definition:
An organic compound containing a functional group with the structure –CHO.
Term: Ketone
Definition:
An organic compound characterized by the presence of the carbonyl functional group within the carbon chain.
Term: Carboxylic Acid
Definition:
An organic compound that contains a carboxyl functional group (-COOH).
Term: IUPAC Naming
Definition:
A systematic method of naming organic chemical compounds established by the International Union of Pure and Applied Chemistry.
Term: Functional Group
Definition:
A specific grouping of atoms within a molecule that is responsible for the chemical properties of that molecule.
These principles of nomenclature and structure not only aid in the identification of these compounds but are also foundational for understanding their reactivity and synthesis in organic chemistry.