Short Summary of IUPAC Nomenclature of Organic Compounds. Introduction. The purpose of the IUPAC system of nomenclature is to establish an international . organic nomenclature are based on the definitive rules published by I.U.P.A.C.1 ( the I.U.P.A.C. Nomenclature for Organic Chemistry, Sections A, B and C. Chemical nomenclature is at least as old as the pseudoscience of alchemy, ( IUPAC) and its Commission on Nomenclature of Organic Chemistry (CNOC).

Organic Chemistry Nomenclature Pdf

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Introduction to Organic Chemistry Nomenclature All organic compounds are made up of at least carbon and hydrogen. Carbon is a special element because it . The IUPAC system of nomenclature was established at various functional classes organic compounds, as well as the relationship between compounds that . vide basic rules and examples for naming monofunctional compounds. However, students of more advanced organic chemistry courses and graduate students.

Acid Halides 18 F. Amides 18 G. Nitriles 19 H. Aldehydes 19 I.

Ketones 21 J. Amines and Ammonium Salts 22 Revised and updated 5. Side chains are not included in the carbon count. It is important that organic compounds are corrrectly and unambiguously named so that there b Name all of the side chains carbon chains attached to the longest chain and list can be absolutely no confusion about what compounds are actually being reported or them in alphabetical order.

There have been many conventions for naming organic compounds - some have 3 , "tetra-" 4 etc. Also ignore "sec-" and "tert-" but not "iso".

The following guidelines for organic nomenclature are based on the definitive rules published by I. CH 3 CH3 2. After this, there is a numerical term of Greek origin followed by the sec-butyl tert-butyl ending "-ane". The first twelve members are given in Table 1. CH3 B.

Worked example 1: Naming the alkanes

More than one double bond Branched side chains are named by renumbering the alkyl group giving the carbon with the a Find and name the longest carbon chain containing the maximum number of free valence i. One double bond C.

This nomenclature is still used in some older texts, c Number the carbon chain giving the double bond the lowest possible location however, the approved nomenclature for alkene stereoisomers involves the prefixes Z- or E-. The d Name side chains in the usual way. For example, a chlorine 5 6 substituent would have a higher priority than a CH3- which in turn would have a higher priority CH3 CH3 Emethylpentene than a H-.

If they are on opposite sides then the prefix is E Cl CH3 Echloromethylpentenol from 'entgegen' meaning 'opposite'. The group priority is then assigned based location number.

Nomenclature of Organic Compounds.pdf

Zchlorobutene The "e" is omitted before a vowel or a "y". The prefixes are as follows: The name of every organic molecule containing a functional group whose name appears as Group Prefix a suffix may be thought of as made up of four parts: F- fluoro Numbers Prefixes Stem Suffix Cl- chloro Locates the Substituents in The name of the Identifes the Br- bromo substituents in alphabetical order pricipal longest principal I- iodo the molecule chain functional group NO2- nitro The Principal Functional Group PFG whose suffix name is used is selected from Table 2 The list is in order of decreasing priority.

Examples Table 2. If you have to take a model to pieces to convert it into another one, then you've got isomers. If you only need to twist it, they are not isomers.

You can use this method to test for isomers. In reality, the reason is that you would have to break the pi bond. Pi bonds are formed by the sideways overlap between p orbitals.

If you tried to rotate the carbon-carbon bond, the p orbitals won't line up any more and so the pi bond is disrupted. This costs energy and only happens if the compound is heated strongly.

In the earliest nomenclature systems, substances were named based on their smell, or their natural source, etc. Since we are only focusing on introductory organic chemistry, i. End with appropriate suffix -ane, -ene, -yne, -yl, -ol, etc.

Identify any branches, called substituents. If there are multiple, different substituents present, name them in alphabetical order e. Prefixes such as di-, tri-, tetra-, etc. If there are several options for choosing the longest continuous carbon chain, choose the one that yields: In summary, the name of the compound is written out with the substituents in alphabetical order followed by the base name derived from the number of carbons in the parent chain.

Commas are used between numbers and dashes are used between letters and numbers. There are no spaces in the name. Related Papers.

By Emmanuel Oche. Introduction to Organic Nomenclature and Functional Groups. By putra saputra. By Kenneth Adu-Gyamfi Ph. By Eulalio Rodriguez. By Mohamed Shorbagi.

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Worked example 1: Naming the alkanes

Need an account? Click here to sign up. Help Center Find new research papers in:There are two branched methyl groups. This compound is an alkyne and will have the suffix -yne. Carbon and its Compounds Preparation of soaps and detergents. This molecule is 1-fluoro-2,2-diiodobutane Naming alcohols ESCKM The rules used to name the alcohols are similar to those already discussed for the hydrocarbons.

Nomenclature of Aldehydes & Ketones

Table 1: Click here to sign up. Specify the exact position of any substituent s by numbering the main chain from the end closest to the substituent could be from left to right, or from right to left! Intro to Organic Chemistry Nomenclature. If there is more than one -CHO group, the suffix is expanded to include a prefix that indicates the number of -CHO groups present -anedial - there should not be more than 2 of these groups on the parent chain as they must occur at the ends.

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