Organic Chemistry Flashcards
(61 cards)
What are all the Reactions of Alkanes
- Cracking
- Combustion
- Chlorination and Bromination (substitution)
Cracking of Alkanes
Alkane -heat/catalyst——> Smaller Alkane + Smaller Alkene
Combustion of Alkanes
Alkane + O2 —ignite excess oxygen—> CO2 + H2O
Chlorination/ Bromination of Alkanes
Alkane+ X2 —–UV Light Energy —-> Haloalkane +HX
All Reactions of Alkenes
- Alkene + Hydrogen Halide —-> Haloalkane
- Alkene —-Acidified H2O —–> Alcohol
- Alkene + X2 —-> Dihaloalkane
- Alkene —-H2—–Pt—> Alkane
- Alkene —-Acidified MnO4- —-REFLUX—–> di-ol
MP/BP of Alkanes
bonded by weak intermolecular forces and are non polar, thus low MP, longer the chain, the higher the mp due to stronger bonds between molecules.
MP/BP of Alkenes
bonded by weak intermolecular forces and are non polar, thus low MP, longer the chain, the higher the mp due to stronger bonds between molecules.
Solubility of Alkanes and Alkenes
Insoluble in Water due to being non polar molecules. Compared to H2O which has slightly negative O and Slightly positive H, so they are not soluble and it is immiscible with water forming two separate layers. Smaller Chain Alkanes are less dense than water and will float on top
Alkene + Hydrogen Halide
Addition Reaction Alkene + Hydrogen Halide —> Haloalkane (Markovniks Rule)
Alkene —-Acidified H2O->
Addition Reaction Alkene —-Acidified H2O —–> Alcohol (Markovniks Rule)
Alkene + X2 —->
Addition Reaction Alkene + X2 —-> Dihaloalkane (Markovniks Rule)
Alkene —-H2—–Pt-heat—->
Alkene —-H2—–Pt—> Alkane Addition Reaction (Markovniks Rule)
Alkene —-Acidified MnO4- —-REFLUX—–>
Oxidation Reaction Alkene —-Acidified MnO4- —-REFLUX—–> di-ol
Alkene —-heat/Dilute H2sO4—–>
Alkene —-heat/Dilute H2sO4—–> Alcohol
why mp/bp increase alkene and alkane chain length
molar mass increases, larger the molar mass, more total valence electrons available, which can randomly cluster to one side of the molecule making an instantaneous polar end - thereby creating a stronger bond to another molecule’s instantaneous polar end
comparison of alkane and alkene mp/bp
each alkene has 2 fewer electrons than the alkane counterpart, thus decreasing the strength in the molecular bonds which decreases the bp of alkenes
requirements for cis trans isomerism
C=C Double Bond (or ring structure):
Prevents rotation, allowing for fixed positions of substituents.
Each carbon of the double bond must have two different groups attached:
If either carbon has two of the same groups, cis–trans isomerism is not possible.
why geometric isomerism
Unlike single bonds, double bonds cannot freely rotate, due to the rigid π (pi) bond. This fixed shape allows different spatial arrangements to be “locked in.”
Alkene —Monomers+heat+catalyst+pressure—>
Alkene —Monomers+heat+catalyst+pressure—>Polymer
Alkene —H+/MnO4- (reflux) —->
Alkene —H+/MnO4- —-> Diol
Haloalkane —-NH3+heat——>
Haloalkane —-NH3+heat——> Amine
Amine Acid or Base
Base
- Turns red litmus blue
turns green UI blue
Haloalkane—–KOH(alc)+heat—->
Haloalkane—–KOH(alc)+heat—-> Alkene
Haloalkane —KOH(aq)+heat—->
Haloalkane —KOH(aq)+heat—-> Alcohol