Question 10.1: Give names for the following compounds: Strategy Use the thr...

Give names for the following compounds:

 

Strategy Use the three-step procedure for naming substituted alkanes: (1) name the parent alkane, (2) number the carbons, and (3) name and number the substituent. (Consult Table 2.4 for parent alkane names.)

Setup (a) This is a five-carbon chain. We can number the carbons starting at either end because the Cl substituent will be located on carbon 3 either way:

(b) This may look like a substituted pentane, too, but the longest carbon chain in this molecule is seven carbons long.

Although Lewis structures appear to be flat and to contain 90° angles, the C atoms in this molecule are all sp³-hybridized (four electron domains around each) and there is free rotation about the C—C bonds [« Section 9.5]. Thus, the molecule can also be drawn as

The substituent is a methyl group on carbon 4.

(c) This is a substituted hexane.

TABLE 2.4 Some Simple Acids
Formula Binary Compound Name Acid Name
HF Hydrogen fluoride Hydrofluoric acid
HCl Hydrogen chloride Hydrochloric acid
HBr Hydrogen bromide Hydrobromic acid
HI Hydrogen iodide Hydroiodic acid
HCN* Hydrogen cyanide Hydrocyanic acid

* Although HCN is not a binary compound, it is included in this table because it is similar chemically to HF, HCl, HBr, and HI.

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(a) 3-chloropentane, (b) 4-methylheptane, (c) 2-methylhexane

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