hydrocarbons Flashcards
alkanes aka? its hybridization, geometry, no of bonds(ethane) bond angle and bond length
alkanes aka paraffins, sp3 hybridization, tetrahedral geometry, 7 sigma bonds in ethane, bond angle is 109 and bond length is 1.54
alkenes aka? its hybridization, geometry, no of bonds(ethene) bond angle and bond length
alkenes aka olefins, sp2 hybridization, trigonal geometry, 5 sigma and 1 pi bond in ethene, bond angle 120 and bond length 1.34
alkynes aka? its hybridization, geometry, no of bonds (ethyne) bond angle and bond length
alkynes aka acetylenes, sp hybridization, linear geometry, 3 sigma and 2 pi bonds in ethyne , bond angle 180 and bond length 1.20
benzene its hybridization, geometry, no of bonds(ethane) bond angle and bond length and m.mass
sp2 hybridization, trigonal geometry, 12 sigma and 3 pi bonds in benzene, bond angle 120 and bond length 1.39. molecular mass is 78
preparation of alkenes (ethene)
1) Dehydration of alcohol (in presence of h2so4)
2) Dehydrohalogenation of alkyl halide (reaction w KOH)
preparation of alkyne (ethyne)
1)Dehydrohalogenation of vicinal dihalide
2)Dehalogenation of tetrahalide
reactions in alkenes/ what type and how many type of reactions?
addition reactions occur in alkenes 6 types
1) Hydration (+ water)
presence of acid catalyst (h2so4)
results in alcohol
2) Hydrogenation (+ hydrogen)
in presence of metal catalyst pt,pd,ni etc
results in ethane
3) Halogenation (+ halogen Br2, Cl2 or I2)
results in dihaloalkanes
4)hydrohalogenation (+ H and X)
results in alkyl halide
5) Halo hydration (+ h2o and X)
results in halohydrin
6) Epoxidation (+ oxygen)
results in epoxide
ozonolysis in alkenes and alkynes
IN ALKENE:
cleavage of alkene by addition of ozone (O3). in presence of zinc. results in ozonide intermediate which then forms aldehyde
IN ALKYNE:
cleavage of alkyne by addition of ozone (o3). results in ozonide intermediate which then become glyoxal
reactions in alkynes/ what type and how many type of reactions?
addition reactions occur in alkynes.
5 types
1)hydrogenation (add hydrogen)
*in presence of metal catalyst like pt pd ni etc)
results in alkene and then alkane
2) hydrohalogenation (+ H and X)
results in dihaloalkane
3) hydration (+water)
in presence of h2so4
results in enol (vinyl alcohol) which rearrange to form aldehyde or ketone.
4)bromination (+ Br2)
results in di bromo ethene and then tetrabromo ethane
addition reactions in benzene
addition and substitution reaction occur in benzene
ADDITION REACTIONS:
1. addition of hydrogen
in presence of Ni catalyst
results in cyclohexane
2. addition of halogen (CL2 or Br2)
in presence of UV light
results in hexahalocyclohexane
substitution reactions in benzene and its types
electrophile substitution of benzene:
involves the replacement of weak electrophile with a strong electrophile.
types of E.S.R (5 types)
1. Nitration
addition of HNO3 (nitric acid)
in presence of h2so4
results in nitrobenzene
- sulphonation
addition of sulphuric acid
results in benzene sulphonic acid - halogenation
addition of halogen
*in presence of lewis acid(fECL2)
results in halobenzene - friedal craft alkylation
addition of alkyl halide in benzene
*in presence of lewis acid (Alcl3)
results in alkyl benzene - friedal craft acylation
addition of acyl halide in benzene
*in presence of lewis acid (Alcl3)
results in arylketone
reason for acidic nature of alkynes
due to 50% s character from sp hybridization.
isomerism and name its types
isomerism is ability of a compound to form isomers. isomers are the compounds with same molecular formula but diff structural formula OR isomers have same number of atoms but diff arrangement of atoms.
2 types
structural isomers and stereo isomers
structural isomers
compounds w same no of atoms but different arrangement of those atom.
4 types
1. chain isomerism
change in the main chain
2. position isomer
change in position of functional group
3. functional grp isomer
change in the functional group
4.metamerism
change in distribution of atom on either side of functional grp.
stereoisomers define only
compounds with same molecular formula but different 3d structure.