Organic Synthesis Reactions And Reagents Flashcards
Alcohol to aldehyde
Distil, K2Cr2O7, H2SO4
Alcohol to ketone
Heat (distil/reflux), K2Cr2O7, H2SO4
Alcohol/aldehyde to COOH
Reflux, K2Cr2O7, H2SO4
Alcohol to chloroalkane (2)
PoCl3 reaction. PCl5, 20 degrees C
HCl, 20 degrees C
Alcohol to bromoalkane
KBr, 50% conc H2SO4, 20 degrees C
Alcohol to alkene
Conc H3PO4, 170 degrees C
Alkene to alcohol
Steam, H3PO4 catalyst, 300 degrees C, 60-70 arm
Alkene to diol
Acidified KMnO4, 20 degrees C
Alkene to alkane
H2, nickel catalyst, 150 degrees c
Alcohol to iodoalkane
‘Red phosphorous’, I2 (make PI3 in situ), reflux
Alcohol to ester (2)
COOH, acid catalyst (H2SO4/HCl), heat
Acyl chloride+ alcohol, reflux
Alkene to halogenoalkane
HX, 20 degrees C
Halogenoalkane to alkene
KOH, ethanol, reflux
Halogenoalkane to COOH
Mg, dry ether, then CO2, then dilute acid
Halogenoalkane to nitrile
KCN, ethanol, reflux
Halogenoalkane to primary amine
Excess ethanolic ammonia, heat
Halogenoalkane to alcohol (2)
Warm aqueous KOH, reflux
Mg, dry ether, then a carbonyl, then dilute acid
Nitrile to primary amine (2)
LiAlH4, the dilute acid
H2, Ni/Pt catalyst, high temp and pressure
Aldehyde/ketone to hydroxynitrile (2)
KCN and H+
KCN, ethanol, reflux
Primary amine to amine
Halogenoalkane
Acyl chloride to primary amide
Conc NH3, 20 degrees C
Acyl chloride to N-substituted amide
Primary amine, 20 degrees C
Acyl chloride to COOH
Cold H2O
Acyl chloride to ester
Alcohol 20 degrees C
Nitrile to COOH
Dilute HCl, reflux
COOH to primary alcohol
LiAlH4
COOH to ester
Alcohol, acid catalyst, heat
COOH to Acyl chloride
PCl5, 20 degrees C
Alkene to dihalogenoalkane
X2 (F2, Cl2, etc.), 20 degrees C
Ester to alcohol
Dilute acid/alkali, reflux
Ester to COOH
Dilute acid/alkali, reflux
Ketone to COOH: RCOCH3 only
I2, NaOH, 20 degrees C