This document discusses IUPAC nomenclature rules for naming organic compounds. It explains that the longest carbon chain is identified as the parent name, such as hexane for a 6-carbon chain. Substituents on the chain are identified and listed alphabetically, such as chloro and methyl groups. The substituents are prefixed with numbers indicating their position on the carbon chain, such as 3-chloro-3,4-dimethylhexane. Examples of correctly named organic compounds are also provided.
NOMENCLATURE OF ORGANIC COMPOUNDS BY -- KHUSH AHUJAKhushAhuja
In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended[1] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). Ideally, every possible organic compound should have a name from which an unambiguous structural formula can be created. There is also an IUPAC nomenclature of inorganic chemistry.
To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple molecules they can be more easily understood than non-systematic names, which must be learnt or looked over. However, the common or trivial name is often substantially shorter and clearer, and so preferred. These non-systematic names are often derived from an original source of the compound. In addition, very long names may be less clear than structural formula.
A nucleophilic aromatic substitution is a substitution reaction in organic chemistry in which the nucleophile exchange a powerful leaving group, such as a halide, on an aromatic ring. There are 6 nucleophilic substitution mechanisms encountered with aromatic systems.
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In chemical nomenclature, the IUPAC nomenclature of organic chemistry is a method of naming organic chemical compounds as recommended[1] by the International Union of Pure and Applied Chemistry (IUPAC). It is published in the Nomenclature of Organic Chemistry (informally called the Blue Book). Ideally, every possible organic compound should have a name from which an unambiguous structural formula can be created. There is also an IUPAC nomenclature of inorganic chemistry.
To avoid long and tedious names in normal communication, the official IUPAC naming recommendations are not always followed in practice, except when it is necessary to give an unambiguous and absolute definition to a compound. IUPAC names can sometimes be simpler than older names, as with ethanol, instead of ethyl alcohol. For relatively simple molecules they can be more easily understood than non-systematic names, which must be learnt or looked over. However, the common or trivial name is often substantially shorter and clearer, and so preferred. These non-systematic names are often derived from an original source of the compound. In addition, very long names may be less clear than structural formula.
A nucleophilic aromatic substitution is a substitution reaction in organic chemistry in which the nucleophile exchange a powerful leaving group, such as a halide, on an aromatic ring. There are 6 nucleophilic substitution mechanisms encountered with aromatic systems.
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1. Naming Hydrocarbons (nomenclature)
2. Drawing Structures: It’s All Good CH3 C H C H CH3 CH3 CH3 CH3 CH CH CH3 2-butene This is called the “condensed structure” C C C C H H H H H H H H CH3 CH CH CH3 On a test, choose a method that shows all Hs CH3CH=CHCH3 Using brackets can also shorten some formulas: CH3CH2CH2CH2CH2CH3 vs. CH3(CH2)4CH3
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2. IUPAC NOMENCLATURE
Let us name this organic compound as an
example.
Cl H
CH3 - CH2 - C – C - CH2 -CH3
CH3CH3
3. How to name organic compounds?
• Find the longest carbon chain. How many
carbon atoms does it have? six.
Thus its parent name : hexane.
• Identify all substituents /branches in the
chain.
• Name these substituents : chloro, methyl.
• Place these in alphabetical order : e.g. chloro,
ethyl, methyl . c,e,m.
4. Naming organic compounds
• If more than one group of a particular type is
present, use prefixes di, tri, tetra, penta etc
(neglect these in alphabetical process!)
e.g. dimethyl, look at m not di.
• No the C atoms in sequence in the longest
chain from the end nearest a branch (give the
lowest no to the substituents) & number the
f.g with the lowest no.
5. Naming organic compunds
• Prefix each substituent by a no showing its
position of attachment to the longest chain
e.g. 3-chloro-3,4-dimethyl instead of 3,4,4.
• Place a dash (hypen) between a no & name.
Place a comma between numbers. Write the
name as one word.
e.g. 3-chloro-3,4-dimethylhexane.