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Simple Organic Compounds: Alkanes Objective lesson 1 chapter 14/15 You will be able to draw, name and list properties of single bonded carbon and hydrogen compounds. Organic Chemistry It is the study of molecular carbon compounds. It does not include carbonates (CO32-), cyanides (CN-), carbon dioxide, or carbon monoxide. The variety of bonds that can be formed by carbon, make it a very versatile element. · Four bonding electrons · Multiple bonds with itself and other elements · Many forms including chains, spheres, tubes, and rings. Functional Groups Special arrangement of atoms that are mainly responsible for the chemical and physical behavior of a molecule. Examples are –OH for alcohols and –COOH for acids. see p. 565 for a list. Example 3-methylpent-2-ene Hydrocarbon chains are named according to the number of carbons in the chain. The first four have prefixes that are different from those learned for molecular compounds. Meth examples -CH4 Eth -C2H6 Prop -C H 3 8 -C4H10 But The remaining have prefixes the same at those learned for molecular compounds. See page 546 of the textbook. You must memorize this list of prefixes. Alkanes This is the simplest of the organic compound families. They are chains of carbon atoms connected by single bonds. The remaining bonding electrons are connected to hydrogen atoms. Since all of the bonding electrons are occupied and single, these are called saturated compounds. Use prefixes shown on page 546 of text, adding -ane. Example: i) 1 carbon has prefix meth. Since this is an alkane we add the ending -ane to obtain methane. ii) 4 carbons have prefix but. Thus it becomes butane. Write the names and draw the structure for C7 H16 and C 3H 8 General Formula The general formula for an alkane is CnH2n+2. Example: i) pentane has 5 carbon atoms, so n=5 and the formula becomes: C5H2(5) + 2 or C5H12 Write the formulae for octane and hexane. Rules to be followed 1: Identify the longest continuous chain to form the root of the name. Example: 2:Identify the branched groups. The prefixes are the same as those for alkanes except they end with -yl. ie. CH3 - methyl group CH2 - CH3 - ethyl group 3: Identify the position of the groups. This is done by counting the carbons in the root chain. Begin labeling the carbons from the end nearest a branch group. Example: 4: If more than one branch is present then name them in alphabetical order. Examples If more than one of a single branch group is present then identify each location and add a prefix of di- or trito indicate the numbers of each group. Example Example Write the structural formula for 3–ethylheptane and 2,2dimethylpropane. Physical Properties (see p. 551) # of carbons Boiling point State and uses 1-4 Less than 30˚C Gases: fuels 5-16 30-275˚C liquids: fuels, plastics 16-22 Greater than 250˚C Heavy liquids: lubricants 18 and over Greater than 400˚C Waxy solids: greases and paraffin waxes 26 or more Greater than 500˚C Solids: asphalts and tars Assignment Read text p. 538-551 Do practice problems 1-9 For a review of chemistry 20 concepts in chemical bonding read p. 532-535 in textbook.