Organic reactions and reaction pathways Flashcards
Alkane reaction - oxidation (combustion)
Alkane + oxygen –> carbon dioxide + water + energy
Alkane reaction - substitution
alkane + halogen – (Uv light present)–> haloalkane + hydrogen halide
Haloalkane reaction - substitution (with halogen)
Haloalkane + halogen– (Uv light present)–> dihaloalkane + hydrogen halide
Haloalkane reaction - substitution (with more reactive halide)
Haloalkane + sodium halide –(ethanol)–> Haloalkane + sodium halide
Haloalkane reaction - substitution (with potassium cynaide)
Haloalkane + potassium cyanide –(heat, ethanol, reflux)–> nitrile + potassium halide
Haloalkane reaction - substation (with ammonia)
Haloalkane +ammonia –(heat, ethanol)–> amine + hydrogen halide
Haloalkane reaction - substation (with dilute sodium hydroxide)
Haloalkane + sodium hydroxide –> alcohol + sodium halide
Haloalkane reaction - Elimination (with concentrated sodium hydroxide)
Haloalkane + sodium hydroxide –(heat)–> alkene + sodium halide + water
Zaitsev’s rule
“poor gets poorer” - the product formed the most is the one where the carbon that loses a hydrogen has the least number of hydrogens to begin with
Alkene reaction - addition (halogenation)
alkene + halogen –> hihaloaklane
Alkene reaction - addition (hydrohalogenation)
Alkene + hydrogen halide –> haloalkane
Markovnikov’s Rule
“Rich get richer” - the product formed the most is the one where the hydrogen atom attaches to the carbon with the most hydrogen atoms.
Alkene reaction - oxidation (combustion)
Alkene + oxygen –> Carbon dioxide + water + energy
Alkene reaction - addition (hydration)
alkene + water –(H3PO4, heat)–> alcohol
Alkene reaction - reduction (hydrogenation)
Alkene + hydrogen –(Ni, heat)–> alkane
Alkene reaction - addition (polymerisation)
alkene + alkene + alkene… –(catalyst, pressure, heat–> polyalkene
Alcohol reaction - oxidation (combustion)
alcohol + oxygen –> carbon dioxide + water + energy
Alcohol reaction - oxidation
1˚ alcohol + oxidising agent –(H+, Cr2O7^2-)–> aldehyde
aldehyde + oxidising agent –(H+, Cr2O7^2-)–> carboxylic acid
2˚ alcohol + oxidising agent –(H+, Cr2O7^2-)–> ketone
3˚ alcohol + oxidising agent –(H+, Cr2O7^2-)–> NR
Alcohol reaction (esterification)
Alcohol + carboxylic acid <–(H+, heat)–> ester + water
Carboxylic acid reaction - condensation (esterification)
alcohol + carboxylic acid <–(H+, heat)–> ester + water
Carboxylic acid reaction - condensation
carboxylic acid + amine –(heat)–> amide + H2O
Acid reactions
Acid + base –> salt + water
Acid + carbonate –> salt + water + carbon dioxide
Acid + metal –> salt + hydrogen
Nitrile reaction - condensation
nitrile + hydrogen –(Ni/Pt, heat)–> amine
amine reaction - condensation
carboxylic acid + amine –(heat)–> amide + water
amine reaction (behaving as an acid)
amine + base –> salt + water