Organic chem Flashcards
Alkanes FRS
Cl2, Br2 in CCl4, UV light
Elimination of alkenes
Conc H2SO4, heat under reflux at 180C or Al2O3, 350C or NaOH/KOH under reflux
ES of alkenes with halogen
X2 in CCl4, in the dark, room temperature
ES of alkenes with water in lab
Conc H2SO4, boil with water
ES of alkenes with water in industrial
steam, conc H3PO4, 300*C, 65atm
Mild oxidation of alkene
KMnO4, NaOH, room temp
diol as product
Strong oxidation of alkene
KMnO4, H2SO4, heat under reflux
terminal alkene: CO2, H2O
ES of arenes to attach -NO2 group
conc H2SO4, conc HNO3, heat at 55*C
ES of arenes to attach -X group
X2 or anhydrous FeX
ES of arenes to attach -CH3 group
CH3Cl, AlCl3
ES of arenes to attach -COCH3 group
CH3COCl, AlCl3
FRS of arenes
Limited Cl2, UV light
Side chain oxidation of arenes (acidic)
KMnO4, dilute H2SO4, heat under reflux
-CH3: puple decolourises
-CH2CH3: purple decolourises, effervescene of CO2
Side chain oxidation of arenes (alkaline)
KMnO4, dilute NaOH, heat under reflux
-CH3: decolourises, brown ppt formed
-CH2CH3: decolourises, brown ppt formed
Ring activating
increase electron density, make benzene ring more reactive
Preparation of halogenoalkane
FRS of alkane: limited Cl2, UV
EA of alkene: dry HX gas, room temp
With alcohol: SOCl2 in pyradine, heat under reflux
PX3, heat / PCl5 at room temp
Mechanism of HA
Sn2: single step
rate=k[Nu][RX]
Sn1: double step
rate=k[RX]
NS of HA with -OH
NaOH/KOH, heat under reflux
R-OH and X- products
NS of HA with CN-
KCN/NaCN, heat under reflux
R-CN and X- products
NS of HA with NH3
Excess NH3 (alc), heat in sealed tube
R-NH2 and HX products
NS of HA with R-OH-Na+
Na(s)/K(s) in ethanol, heat
R-O-R’ and NaX as product
Reduction of R-CN with H2/[H]
H2, Ni, heat, high pressure
R-CH2NH2 prodct
LiAlH4 in dry ether, reflux
same product
Acidic hydrolysis of HA
HCl/H2SO4, heat under reflux
R-COOH and NH4+ prduct
Alkaline hydrolysis of HA
NaOH/KOH, heat under reflux
R-COO- and NH3 product