Alcohol=OH. Aldehyde=CHO (H on carbonyl). Ketone=CO (no H on carbonyl). Carboxylic acid=COOH. Amine=NH2. These 5 appear on almost every orgo exam.
⚗️ Functional Groups
WANE — Water solubility rule
Solubility of Functional Groups
Groups that form H-bonds with water are water soluble. Alcohols, amines, carboxylic acids — all soluble in small molecules. As carbon chain grows, hydrophobic character WANES solubility.
⚗️ Functional Groups
'Carbonyls are electrophiles at C, nucleophiles at O'
Carbonyl Reactivity
The carbonyl carbon (C=O) is electron-deficient — nucleophiles attack here. The oxygen is electron-rich — it can donate electrons. This determines ALL carbonyl reaction mechanisms.
Electron Withdrawing Groups (EWG): NO2, CN, halogens — pull density away from ring, deactivate. Electron Donating Groups (EDG): OH, NH2, alkyl — push density into ring, activate.
⚗️ Functional Groups
Priority order for IUPAC naming: carboxylic acid > ester > amide > aldehyde > ketone > alcohol > amine
Functional Group Priority in IUPAC Naming
When a molecule has multiple functional groups, the highest priority group determines the suffix (parent name). Priority order (highest to lowest): carboxylic acid (-oic acid) > ester (-oate) > amide (-amide) > aldehyde (-al) > ketone (-one) > alcohol (-ol) > amine (-amine). Lower priority groups become prefixes (e.g., amino-, hydroxy-, oxo-). Only one suffix allowed — pick the highest priority group.
Highest
Carboxylic acid — suffix -oic acid
Next
Ester (-oate), Amide (-amide)
Then
Aldehyde (-al), Ketone (-one)
Lower
Alcohol (-ol), Amine (-amine)
Lowest
Alkene (-ene), Alkyne (-yne), Alkane (-ane)
⚗️ Functional Groups
Leaving group ability: I⁻ > Br⁻ > Cl⁻ > F⁻ — opposite of nucleophilicity in polar protic
Leaving Group Ability
A good leaving group departs as a stable anion. Stability = weak base = conjugate of strong acid. Order: I⁻ (best) > Br⁻ > Cl⁻ > F⁻ (worst). Tosylate (OTs) and mesylate (OMs) are excellent leaving groups — convert OH to a good LG. OH⁻ and NH₂⁻ are poor leaving groups (strong bases). Protonation converts OH to H₂O (good LG) — acid catalysis. In SN2: I⁻ > Br⁻ > Cl⁻ >> F⁻.
Best LGs
I⁻, TsO⁻, MsO⁻, TfO⁻ — weakest bases
Good LGs
Br⁻, Cl⁻, H₂O (protonated OH)
Poor LGs
F⁻, OH⁻, OR⁻, NH₂⁻ — too basic
Trick
Protonate OH with acid → H₂O (good LG)
⚗️ Functional Groups
Nucleophilicity vs basicity: in polar protic — larger atom = better nucleophile despite weaker base
Nucleophilicity Trends
Nucleophilicity = rate of attack on electrophile. In polar protic solvents: I⁻ > Br⁻ > Cl⁻ > F⁻ (opposite of basicity — larger, less solvated atoms are better nucleophiles). In polar aprotic solvents: follows basicity order (F⁻ best nucleophile). Negatively charged > neutral. Less sterically hindered = better nucleophile. Good nucleophiles are not always good bases: RS⁻ (excellent nucleophile, weak base), PhO⁻ (moderate nucleophile, weak base).
⚗️ Functional Groups
Degree of unsaturation (DoU): rings and pi bonds — DoU = (2C+2+N-H-X)/2
Degrees of Unsaturation in Detail
DoU formula: (2C + 2 + N – H – X) / 2. Oxygen does not appear (no net effect). Examples: C₆H₆ (benzene) = (12+2-6)/2 = 4 DoU (3 double bonds + 1 ring). C₄H₈ = (8+2-8)/2 = 1 DoU (one ring or one double bond). C₄H₄ = (8+2-4)/2 = 3 DoU. If DoU ≥ 4 with 6 carbons → likely aromatic ring. DoU = 0 → fully saturated. Nitrogen adds 1 to numerator; halogens subtract like H.
⚗️ Functional Groups
Tautomers vs resonance structures: tautomers are different compounds; resonance are same compound
Tautomers vs Resonance Structures
Resonance structures: same compound, same atom positions, only electrons differ — connected by double-headed arrow (↔). Tautomers: different compounds, atoms in different positions (usually H moves) — connected by equilibrium arrow (⇌). Example: keto ⇌ enol tautomers (H moves from C to O). Resonance structures cannot be separated; tautomers can be separated (in principle, often fast equilibrium). Both described as 'contributing structures' or 'forms' but mean fundamentally different things.
⚗️ Functional Groups
Inductive vs resonance effects: inductive = through sigma bonds; resonance = through pi system
Inductive vs Resonance Electronic Effects
Inductive effect: electron withdrawal or donation through sigma bonds. Decreases with distance (drops off as 1/r²). Example: Cl withdraws electrons inductively — makes alpha carbon electrophilic. Resonance effect: delocalization through pi bonds/conjugation. Does not drop off with distance within conjugated system. Example: -NO₂ withdraws by resonance ortho/para to itself. Compounds can have both effects working together or in opposition (e.g., halogens: withdraw inductively, donate by resonance).
⚗️ Functional Groups
Sigma bond = head-on overlap; pi bond = side-by-side overlap — pi bonds rotate only by breaking
Sigma and Pi Bonding
Sigma (σ) bonds: head-on orbital overlap, single bonds, freely rotating, always present in any bond. Pi (π) bonds: side-by-side p orbital overlap, present in double and triple bonds, restrict rotation. Double bond = 1σ + 1π. Triple bond = 1σ + 2π. Pi bonds are weaker than sigma bonds (less overlap), more reactive, and responsible for E/Z isomerism (restricted rotation). Electrophiles attack pi bonds preferentially.
⚗️ Functional Groups
Intermolecular forces: H-bond > dipole-dipole > London dispersion — affect BP and solubility
Intermolecular Forces & Physical Properties
H-bonding: requires N-H, O-H, or F-H + lone pair — strongest IMF after covalent/ionic. Alcohols, carboxylic acids, amines (N-H). Dipole-dipole: polar molecules without H-bond donors (ketones, aldehydes, ethers, esters). London dispersion (van der Waals): all molecules — increases with size/surface area. Boiling point: H-bond >> dipole > dispersion. Water solubility: functional groups that H-bond with water are soluble; long carbon chains reduce solubility.
Q: What are the Big 5 functional groups and their structures?
A: Alcohol: R-OH. Aldehyde: R-CHO (carbonyl carbon has one H). Ketone: R-CO-R' (carbonyl carbon has two R groups, no H). Carboxylic acid: R-COOH. Amine: R-NH₂. These five appear on almost every organic chemistry exam. The suffix gives the functional group: -ol (alcohol), -al (aldehyde), -one (ketone), -oic acid (carboxylic acid), -amine (amine).
Q: How do you identify functional groups using IR spectroscopy?
Q: Why is the carbonyl carbon electrophilic and the oxygen nucleophilic?
A: In C=O, oxygen is more electronegative — it pulls electron density from carbon, making carbon electron-deficient (electrophilic). Nucleophiles attack the carbonyl carbon. The oxygen retains lone pairs and electron density — making it nucleophilic (can donate electrons). This determines all carbonyl reaction mechanisms: nucleophilic addition to the carbon, protonation at oxygen.
Q: What is the difference between EWG and EDG, and how do they affect reactivity?
A: Electron-withdrawing groups (EWG: NO₂, CN, halogens, COOH): pull electron density away from the ring or adjacent atoms, stabilize anions, increase acidity, deactivate aromatic rings, direct meta in EAS. Electron-donating groups (EDG: OH, NH₂, OR, alkyl): push electron density into adjacent systems, destabilize anions (decrease acidity), activate aromatic rings, direct ortho/para in EAS.
Q: How does water solubility relate to functional groups?
A: Groups that form H-bonds with water are water soluble. Alcohols, amines, carboxylic acids, and ketones/aldehydes (via dipole interactions) dissolve in water for small carbon chains. As the carbon chain grows, hydrophobic character dominates and solubility decreases. Carboxylic acids become water-soluble salts (RCOONa) under basic conditions — this is used in separations.
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