Interpretation:
The structures of all possible organic products that can form when the alcohol 3-methyl-3-hexanol undergoes dehydration has to be drawn.
Concept Introduction:
Dehydration reaction is the loss of water from a single reactant. Alcohol undergoes dehydration reaction to form
Want to see the full answer?
Check out a sample textbook solutionChapter 14 Solutions
Study Guide with Selected Solutions for Stoker's General, Organic, and Biological Chemistry, 7th
- The alcohol 2,2- dimethyl-1- butanol cannot dehydratedarrow_forwardDraw the skeletal structure for the product that forms when the alcohol 2,2-dimethyl-1-pentanol is oxidized. OHarrow_forwardEach of the following alcohols is named incorrectly. However, the names give correct structural formulas. Draw structural formulas for the compounds, and then write the correct IUPAC name for each alcohol. a. 2-Ethyl-1-propanol b. 2,4-Butanediol c. 2-Methyl-3-butanol d. 1,4-Cyclopentanediolarrow_forward
- What functional group distinguishes each of the following hydrocarbon derivatives? a. halohydrocarbons b. alcohols c. ethers d. aldehydes e. ketones f. carboxylic acids g. esters h. amines Give examples of each functional group. What prefix or suffix is used to name each functional group? What are the bond angles in each? Describe the bonding in each functional group. What is the difference between a primary, secondary, and tertiary alcohol? For the functional groups in ah, when is a number required to indicate the position of the functional group? Carboxylic acids are often written as RCOOH. What does COOH indicate and what does R indicate? Aldehydes are sometimes written as RCHO. What does CHO indicate?arrow_forwardWrite a general equation showing the preparation of a carboxylic acid from an alcohol.arrow_forwardBoth aldehydes and ketones contain carbonyl groups. In aldehydes, the carbonyl carbon atom is bonded to a hydrogen atom, whereas in ketones, the carbonyl carbon atom is bonded to another carbon atom. Select the true statements about aldehydes and ketones. - Ketones have lower boiling points than alcohols of similar size. - Aldehydes contain a carbon–oxygen double bond. - Butanal has a higher boiling point than 2-butanol. - Aldehydes with more than five carbon atoms are soluble in water, but not organic solvents. - Both aldehydes and ketones can hydrogen bond with water molecules. - Propanal is a gas at room temperature, whereas formaldehyde (methanal) is a liquid at room temperature.arrow_forward
- Arrange these compounds in order of increasing solubility in water. Diethyl ether Нехane Ethylene glycol dimethyl etherarrow_forwardwhat is the oxidation of 2-propanolarrow_forwardWhich class of compounds shows H-bonding even more than in alcohols? aldehydes carboxylic acids phenols ethersarrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningIntroductory Chemistry: An Active Learning Approa...ChemistryISBN:9781305079250Author:Mark S. Cracolice, Ed PetersPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningWorld of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning