Download presentation
Presentation is loading. Please wait.
Published byRose Walters Modified over 9 years ago
1
Ch 10.5 Functional Groups
2
Definition Functional Groups Have specific name/formula/structure Carry out specific Rx Have specific characteristics a)If they contain O, S, N: makes molecule polar, higher MP/BP, soluble in water, liquid/solid at RT b)If they contain C and H only: makes molecule non-polar, low MP/BP, soluble in organic solvents, gases at RT
3
Alk-anes, enes, ynes Hydrocarbons with single, double, triple bonds C-C or C=C or C=C Caution: add enough Hydrogen to fill remaining covalent bonds CH3-CH3 or CH2=CH2 or CH=CH
4
Aromatic HC Molecules containing Benzene rings substituent called Phenyl
5
Alcohols Contain hydroxyl group - OH Example: Ethanol
6
Ethers Oxygen bridge in a carbon skeleton C-O-C Example: Diethyl ether
7
Aldehyde Contain Carbonyl group: O double bonded to Carbon C=O located at the end of Carbon skeleton Example: Propanal
8
Ketone Carbonyl at a center Carbon Example: Propanone
9
Amine Contains Nitrogen Three different types of amines Primary – NH2 attached to 1 C and two H Secondary C-NH-C attached to two C and one H Tertiary C-N-C attached to three C, no H! C Raises pH of a solution
10
Carboxylic Acids Carboxyl =Alcohol and Carbonyl group at the same carbon Lowers pH of solution! Example: Ethanoic Acid
11
Ester Carboxylic Acid in the center of a molecule Ethyl ethanoate
12
Amide Like Carboxyl group, OH replaced by NH2 Ethanamide
13
Thiol Thiol group -SH Ethane thiol
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.