Compare and interpret the infrared spectra of 4-methylcyclohexene and 4-methylcyclohexanol.

Using the relationship between the structure and the boiling point. Obtain a table for the listed chemicals below showing how the boiling point will be different with (1) the different chemical structures, (2) with different functional groups. Boiling Point and Functionalized Compounds: Chemical: Cyclohexanol Cyclohexanone Cyclohexene Benzaldehyde Benzyl alcohol

Draw the structure of the following compounds: 3-bromo-1-cyclopropyl-2-methylbutane 2-hydroxycyclopentane 3-isopropoxypentane 4-hydroxypentanoic acid

For each IUPAC name, draw the corresponding structural formula and line-angle formula. (a) Ethanol (b) Butanal (c) Butanoic acid (d) Ethanoic acid (e) Heptanoic acid (f) Propanoic acid (g) Octanal (h) Cyclopentene (i) Cyclopentanol (j) Cyclopentanone (k) Cyclohexanol (l) Propanone

Aldehydes and ketones react with one molecule of an alcohol to form compounds called hemiacetals, in which there is one hydroxyl group and one ether-like group. Reaction of a hemiacetal with a second molecule of alcohol gives an acetal and a molecule of water. We study this reaction in Chapter 16. Draw structural formulas for the hemiacetal and acetal formed from these reagents. The stoichiometry of each reaction is given in the problem.

cyclohexanol bond line structure

The relationship between functionality and boiling point of Cyclohexanol, Cyclohexanone, Cyclohexene, Benzaldehyde and Benzyl alcohol

Draw the structures of a homologous series of alcohols that have from one to six carbons and give each of them a common name and a systematic name.

Write the common (not IUPAC) name and standard abbreviation for each molecule. o 9=8-0 O-CH, H O=d-0 H H O=d-0 OH H انه H O-CHO H 9 H H OH H N Fo H H OH H H NH NH NH₂ H NH₂ Name: 0 Abbreviation: 0 Name: 1 Abbreviation: 0 Name: 0 Abbreviation: 0

1. Write in the correct reagents to accomplish these reactions. a) 2-methylcyclohexanol b) benzyl alcohol → 1-bromo-2-methylcyclohexane benzaldehyde