Aldehydes, Ketones and Carboxylic Acids — Concept Maps
ICSE · Class 12 · Chemistry
4 concept maps of Aldehydes, Ketones and Carboxylic Acids for ICSE Class 12 Chemistry, each also written out as a text outline.
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Comprehensive Overview of Aldehydes, Ketones, and Carboxylic Acids
The map in words
- root((Carbonyl & Carboxyl
- Compounds))
- Aldehydes
- Structure
- R-CHO
- Carbonyl at end
- Preparation
- From primary alcohols
- From alkynes
- Reactions
- Nucleophilic addition
- Oxidation to acids
- Reduction to alcohols
- Tests
- Tollens test
- Fehling test
- Structure
- Ketones
- Structure
- R-CO-R
- Carbonyl in middle
- Preparation
- From secondary alcohols
- Friedel-Crafts acylation
- Reactions
- Nucleophilic addition
- Oxidation with cleavage
- Reduction to alcohols
- Properties
- Less reactive
- No Tollens test
- Structure
- Carboxylic Acids
- Structure
- R-COOH
- Acidic group
- Acidity
- Weak acids
- Resonance stabilization
- Ka 10-4 to 10-5
- Preparation
- From aldehydes
- From nitriles
- From Grignard + CO2
- Derivatives
- Acid chlorides
- Anhydrides
- Esters
- Amides
- Reactions
- Esterification
- Acyl substitution
- Decarboxylation
- Salt formation
- Structure
- Aldehydes
Aldehydes, Ketones and Carboxylic Acids - Complete Overview
The map in words
- Carbonyl Compounds
- Aldehydes
- Structure
- R-CHO
- Carbonyl at end of chain
- Properties
- More reactive than ketones
- Easily oxidized
- Lower bp than alcohols
- Reactions
- Nucleophilic addition
- Oxidation to acids
- Reduction to alcohols
- Aldol condensation
- Structure
- Ketones
- Structure
- R-CO-R
- Carbonyl within chain
- Properties
- Less reactive than aldehydes
- Harder to oxidize
- Similar bp to aldehydes
- Reactions
- Nucleophilic addition
- Clemmensen reduction
- Wolff-Kishner reduction
- Haloform reaction
- Structure
- Carboxylic Acids
- Structure
- R-COOH
- Carboxyl group
- Properties
- Weak acids pKa 3-5
- Form dimers
- Very soluble when low MW
- Reactions
- Esterification
- Formation of derivatives
- Decarboxylation
- Alpha halogenation
- Derivatives
- Acid chlorides
- Acid anhydrides
- Esters
- Amides
- Structure
- Aldehydes
Carboxylic Acids — Complete Concept Map
The map in words
- root((Carboxylic Acids
- RCOOH))
- Preparation
- Oxidation of
- Primary Alcohols
- Aldehydes
- Nitrile Hydrolysis
- One Carbon MORE
- Grignard plus CO2
- One Carbon MORE
- Ester Hydrolysis
- Acid or Alkaline
- Koch Reaction
- Alkene plus CO plus H2O
- Alkylbenzene Oxidation
- Any chain gives COOH
- Oxidation of
- Physical Properties
- Boiling Points Very High
- Cyclic Dimer Formation
- Double H-bonds
- Solubility
- Decreases after C4
- H-bonding with water
- Melting Points
- Alternating Pattern
- Even C higher than Odd C
- Boiling Points Very High
- Acid Strength
- Measured by Ka and pKa
- Order
- Mineral Acids
- Carboxylic Acids
- Phenols
- Alcohols
- Electron Withdrawing Groups
- Increase Acid Strength
- F Cl Br I CN NO2
- Electron Releasing Groups
- Decrease Acid Strength
- Alkyl Groups
- Key Order
- HCOOH Greater PhCOOH Greater CH3COOH
- Chemical Reactions
- Acidic Reactions
- With NaHCO3 gives CO2
- With metals gives H2
- With NaOH gives salt
- Forming Derivatives
- Acid Chloride via PCl5 SOCl2
- Ester via ROH H2SO4
- Amide via NH3 then heat
- Anhydride via P2O5
- Decarboxylation
- Sodalime gives alkane
- Kolbes Electrolysis R-R
- Hunsdiecker gives RBr
- HVZ Reaction
- Alpha halogenation
- Cl2 or Br2 with red P
- Benzene Ring Reactions
- Meta directing
- Deactivating group
- No Friedel Crafts
- Acidic Reactions
- Preparation
Carbonyl Compounds and Carboxylic Acids
The map in words
- Carbonyl Compounds and Carboxylic Acids
- Aldehydes
- Ketones
- Carboxylic Acids
- Functional Derivatives of Carboxylic Acids
- Methods of Preparation
- Acidity and Resonance
- Reduction and Oxidation
- Decarboxylation and Descent
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