Study Aids:
Click the Study Aids tab at the bottom of the book to access your Study Aids (usually practice quizzes and flash cards).
Study Pass:
Study Pass is our latest digital product that lets you take notes, highlight important sections of the text using different colors, create "tags" or labels to filter your notes and highlights, and print so you can study offline. Study Pass also includes interactive study aids, such as flash cards and quizzes.
Highlighting and Taking Notes:
If you've purchased the All Access Pass or Study Pass, in the online reader, click and drag your mouse to highlight text. When you do a small button appears – simply click on it! From there, you can select a highlight color, add notes, add tags, or any combination.
Printing:
If you've purchased the All Access Pass, you can print each chapter by clicking on the Downloads tab. If you have Study Pass, click on the print icon within Study View to print out your notes and highlighted sections.
Search:
To search, use the text box at the bottom of the book. Click a search result to be taken to that chapter or section of the book (note you may need to scroll down to get to the result).
View Full Student FAQs
14.7 Phenols
Learning Objective
- Describe the structure and uses of some phenols.
Compounds in which an OH group is attached directly to an aromatic ring are designated ArOH and called phenolsAn aromatic compound with an OH group attached directly to a benzene ring.. Phenols differ from alcohols in that they are slightly acidic in water. They react with aqueous sodium hydroxide (NaOH) to form salts.
ArOH(aq) + NaOH(aq) → ArONa(aq) + H2OThe parent compound, C6H5OH, is itself called phenol. (An old name, emphasizing its slight acidity, was carbolic acid.) Phenol is a white crystalline compound that has a distinctive (“hospital smell”) odor.
To Your Health: Phenols and Us
Phenols are widely used as antiseptics (substances that kill microorganisms on living tissue) and as disinfectants (substances intended to kill microorganisms on inanimate objects such as furniture or floors). The first widely used antiseptic was phenol. Joseph Lister used it for antiseptic surgery in 1867. Phenol is toxic to humans, however, and can cause severe burns when applied to the skin. In the bloodstream, it is a systemic poison—that is, one that is carried to and affects all parts of the body. Its severe side effects led to searches for safer antiseptics, a number of which have been found.
One safer phenolic antiseptic is 4-hexylresorcinol (4-hexyl-1,3-dihydroxybenzene; resorcinol is the common name for 1,3-dihydroxybenzene, and 4-hexylresorcinol has a hexyl group on the fourth carbon atom of the resorcinol ring). It is much more powerful than phenol as a germicide and has fewer undesirable side effects. Indeed, it is safe enough to be used as the active ingredient in some mouthwashes and throat lozenges.
(a) Phenolic compounds help to ensure antiseptic conditions in hospital operating rooms. (b) The compound 4-hexylresorcinol is mild enough to be used as the active ingredient in antiseptic preparations for use on the skin.
Source: Photo © Thinkstock
Concept Review Exercises
-
How do phenols differ from alcohols in terms of structure and properties?
-
How do phenols differ in properties from aromatic hydrocarbons?
Answers
-
Phenols have an OH group attached directly to an aromatic ring. Phenols are weakly acidic.
-
Phenols have an OH group and are somewhat soluble in water.
Key Takeaways
- Phenols are compounds in which an OH group is attached directly to an aromatic ring.
- Many phenols are used as antiseptics.
Exercises
-
Name each compound.
-
-
Name each compound.
-
-
Draw the structure for each compound.
- m-iodophenol
- p-methylphenol (p-cresol)
-
Draw the structure for each compound.
- 2,4,6-trinitrophenol (picric acid)
- 3,5-diethylphenol
Answers
-
- o-nitrophenol
- p-bromophenol
-
-
-
-
