Alphatic Reactions Conditions 2 Flashcards
CH2CH2 → CH3CH2Br
electrophilic addition using HBr
CH3CH2OH → CH3COOH
oxidation using K2Cr2O7(aq) with H2SO4(aq), heat under reflux
CH3CH2Br → CH3CH2OH
nucleophilic substitution using KOH(aq) or NaOH(aq), heat under reflux
CH3CH2Br → CH2CH2
elimination using KOH in ethanol or NaOH in ethanol
CH3CN → CH3CH2NH2
reduction using NaBH4(aq) or LiAlH4 in dry ether followed by HCl(aq)
C6H6 → C6H5CH3
electrophilic substitution using CH3Cl and AlCl3 catalyst (Friedel–Crafts reaction)
CH3CHO → CH3CH(OH)(CN)
nucleophilic addition using HCN
CH3COOH → CH3COO–Na+
acid–base reaction using NaOH(aq) or NaHCO3(aq)
CH3CH2NH2 → CH3CH2NH3+
acid–base reaction using any dilute acid
CH2CH2 → CH3CH2OH
hydration using concentrated sulfuric acid followed by dilution with water
CH3COOH → CH3COOCH2CH2CH3
esterification (or condensation) using CH3CH2CH2OH with conc. H2SO4 catalyst
Deduce the reaction type from the reagent, then deduce the product.
(conc. H2SO4)
CH<sub>3</sub>CH<sub>2</sub>OH(l) → ………………
dehydration to CH2CH2 (ethene)
Deduce the reaction type from the reagent, then deduce the product.
(KOH(aq))
CH<sub>3</sub>CH<sub>2</sub>Br(l)→ ………………
nucleophilic substitution to form CH3CH2OH (ethanol)
Deduce the reaction type from the reagent, then deduce the product.
(KOH in ethanol)
CH<sub>3</sub>CH<sub>2</sub>Br(l) → ………………
elimination to form CH2CH2 (ethene)
Deduce the reaction type from the reagent, then deduce the product.
(LiAlH4 in dry ether, then add dilute HCl(aq))
CH<sub>3</sub>COOH(l) → ………………
reduction to CH3CH2OH (ethanol)