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Organic Chemistry 1 - Nomenclature, Dr Rivera

by: Abigail Mitchell

Organic Chemistry 1 - Nomenclature, Dr Rivera 3600

Marketplace > Georgia College & State University > Chemistry > 3600 > Organic Chemistry 1 Nomenclature Dr Rivera
Abigail Mitchell
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About this Document

Nomenclature characteristics for alkanes, cycloalkanes, alkyl halides, ethers, alcohols, and amines. Also, includes functional groups
Organic Chemistry
Dr. Rivera
Class Notes
Organic Chemistry, nomenclature, functional groups, Alkanes, Cycloalkanes, alkylhalides, Ethers, alcohols, amines




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This 2 page Class Notes was uploaded by Abigail Mitchell on Monday October 17, 2016. The Class Notes belongs to 3600 at Georgia College & State University taught by Dr. Rivera in Fall 2016. Since its upload, it has received 8 views. For similar materials see Organic Chemistry in Chemistry at Georgia College & State University.


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Date Created: 10/17/16
Organic Chemistry - Nomenclature Dr. Rivera CH 3 Alkanes - Compounds composed of only single carbons and hydrogen atoms connected by single bonds - Nonpolar, low solubility, LDS intermolecular forces C n 2n+2 Cycloalkanes - Cyclo means has a ring - Van der Waal intermolecular forces - Nonpolar, low melting and boiling points C n 2n Alkyl Halides - Add suffix –ide to the end of the halogen name CH 3  Methyl fluoride - Typically quite polar - Participate in SN1 and SN2 reactions Ethers - Name of carbon chain followed by suffix –oxy CH 3-  Methoxy - Polar, dipole-dipole interactions, H-bonding, soluble Alcohols - Name of carbon chain followed by suffix –ol CH 3H  Methanol - Polar from O – H bond, high melting point, low boiling point (flammable), high solubility Amines - Replace the “e” in the carbon chain name with “amine” - A primary amine has one alkyl group attached to the nitrogen - A secondary amine has 2 alkyl groups attached to the nitrogen - A tertiary amine has 3 alkyl groups attached to the nitrogen - Polar, H-bonding, high melting and boiling points


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