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ALKANES
Contain single bonds
CH3-CH2-CH2-CH3
Saturated hydrocarbon
Substitution reaction
Cycloalkanes
If the carbon chain that forms the straight-chain hydrocarbon is long enough, the two ends coming together to form a cycloalkane.
One hydrogen atom has to be removed from each end of the hydrocarbon chain to form the CC bond that closes the ring.
Cycloalkanes therefore have two less hydrogen atoms than the parent alkane and a generic formula of CnH2n.
Examples of cycloalkanes
The smallest alkane that can form a ring is cyclopropane, C3H6, in which the
three carbon atoms lie in the same plane.
The angle between adjacent CC bonds is only 60° as seen in the model below:
Molecular models of cycloalkanes:
cyclohexane cyclopropane
cyclobutane cyclopentane
Name the following:
The following compound, for example, is a derivative of pentane because the longest chain contains five carbon atoms:
Thus, its name is 2-methylpentane
Naming the cycloalkanes:
Find the longest continuous loop of carbon atoms in the skeleton structure.
Name the compound as a derivative of the cycloalkane with this number of carbon atoms: 3-C = cyclopropane 4-C = cyclobutane 5-C = cyclopentane
Name the following cycloalkanes:
Rings (or cyclic compounds) are composed of rings of carbon and sometimes oxygen or nitrogen. For example, cyclohexane has a ring of six carbon atoms.
cyclopropane cyclobutane cyclopentane
cyclohexanebromocyclohexane cyclohexenecyclohexane
Name the Alkane compound with an -yne ending for a triple
bond.
The alkane methane as an alkyne….
What is it’s name ?
methyne
The aromatic hydrocarbons:
Benezene is good example: C6H6
Interior ring formed by three double C-C bonds
Also called a benzene ring
The carboxylic acids:
Carboxylic acids contain the carboxyl group, which is a contraction of the carbonyl and hydroxyl names since carboxylic acids contain both groups attached to one carbon.
Often written as: RCOOH or RCO2H
IUPAC NomenclatureCarboxylic acids are named by replacing the -e of the alkane root name with -oic and adding the word acid. Substituents on the chain are named as usual.
IUPAC naming of acids:The table below gives common and IUPAC names for some of the simple carboxylic acids.
IUPAC Name Common Name Formula
methanoic acid formic acid HCOOH
ethanoic acid acetic acid CH3COOH
propanoic acid propionic acid CH3CH2COOH
butanoic acid butyric CH3(CH2)2COOH
pentanoic acid valeric CH3(CH2)3COOH
Ethers R-O-R/
If R=R/ symmetrical CH3-O-CH3
Dimethyl ether CH3-O-CH2CH3
Ethylmethyl ether Non-polar solvents
ALDEHYDES
O Carbonyl group –C—
O H - C -H Methanal
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http://www.chem.uni.edu/~macmilla/mcmurry/mcmurry_chapter_19a/sld001.htm
Formed by a reaction of an acid and an alcohol.
Ester structure
Conversion of acids into esters is called esterification.