
Concept explainers
(a)
Interpretation:
State True or false.
The two most important reactions of alcohols are their acid-catalyzed dehydration to give
Concept Introduction:
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
True.
Explanation of Solution
Alcohols are organic compounds containing -OH group. It undergoes in the presence of acid to form an alkene. Dehydration is the removal of water from alcohol.
Alcohols undergo oxidation to yield aldehyde, ketone, and carboxylic acid. The primary alcohol in an acid catalyzed oxidation gives an aldehyde and further acid catalyzed oxidation gives a corresponding acid.
The secondary alcohol in an acid catalyzed oxidation fives a ketone.
Therefore, this statement is True.
(b)
Interpretation:
State True or false.
The acidity of alcohols is comparable to that of water.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
True.
Explanation of Solution
The strength of an acid can be measured by the acid dissociation constant Ka while the pKa value is logarithmic value of the acid dissociation constant. So, the alcohol has the nearly same pKa value as of water.
Therefore, this statement is True.
(c)
Interpretation:
State True or false.
Water-insoluble alcohols and water-insoluble phenols react with string bases to give water soluble salts.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
False.
Explanation of Solution
Alcohol is a water-soluble compound. It is soluble in water because of the hydrogen bonding between oxygen and hydrogen atoms of water and alcohol molecules. Phenol is also water soluble because of hydrogen bonding. Water-soluble alcohol and water-insoluble phenol react with string bases to form water-soluble salt.
Therefore, this statement is False.
(d)
Interpretation:
State True or false.
Acid catalyzed dehydration of cyclohexanol gives cyclohexene.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
False.
Explanation of Solution
Acid-catalyzed dehydration of cyclohexanol gives corresponding alkene. In the presence of sulfuric acid, cyclohexanol gives cyclohexene.
Therefore, this statement is False.
(e)
Interpretation:
State True or false.
When the acid-catalyzed dehydration of an alkene can yield isomeric alkenes, the alkene with the greater number of hydrogens in the carbons of the double bond generally predominates.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
False.
Explanation of Solution
Acid-catalyzed dehydration of an alcohol gives an isomeric alkene. The isomeric alkene, which has a lower number of hydrogen atoms in the double bond, has a grater yield. Hence, when butanol undergoes an acid-catalyzed dehydration, 2-butene is the major product.
Therefore, this statement is False.
(f)
Interpretation:
State True or false.
The acid-catalyzed dehydration of 2-butanol gives predominantly 1-butene.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
False.
Explanation of Solution
An acid catalyzed dehydration of butanol gives predominantly 2-butene. The yield of 1-butene is approximately because in the acid-catalyzed dehydration reaction of an alcohol, the major product has the lower number of hydrogen atoms attached to the carbon atoms with double bonds. Thus, 2-Butene is the major product.
Therefore, this statement is False.
(g)
Interpretation:
State True or false.
The oxidation of a primary alcohol gives either an aldehyde or a carboxylic acid depending on experimental conditions.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
True.
Explanation of Solution
The oxidation of the primary alcohols gives either aldehyde or carboxylic acid, depending on the experimental condition. For illustration, the primary alcohol in an acid catalyzed oxidation gives an aldehyde and further acid catalyzed oxidation gives a corresponding acid.
Therefore, this statement is True.
(h)
Interpretation:
State True or false.
The oxidation of a secondary alcohol gives a carboxylic acid.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
False.
Explanation of Solution
The secondary alcohol in an acid-catalyzed oxidation gives ketone. The oxidation of the secondary alcohol gives ketone in the presence of potassium chromate as an oxidizing agent. It does not produce carboxylic acid because it lacks a hydrogen atom.
Therefore, this statement is false.
(i)
Interpretation:
State True or false.
Acetic acid, CH3 COOH, can be prepared from ethylene, CH2 =CH2, by treatment of ethylene with H2 O/H2 SO4, followed by treatment with K2 Cr2 O7 /H2 SO4.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
True.
Explanation of Solution
Ethylene undergoes acid catalyzed hydration to produce ethanol. This, ethanol, in further treatment with potassium dichromate, undergoes oxidation to form acetic acid. The reaction is.
Therefore, this statement is True.
(j)
Interpretation:
State True or false.
Treatment of propene, CH3 CH=CH2, with H2 O/H2 SO4, followed by treatment with K2 Cr2 O7 /H2 SO4 gives propanoic acid.
Concept Introduction:
Chemical reaction is the procedure to transform the chemical substance in the new substance. During this procedure sometimes, acid is involved which is the substance which could either accept electron pairs or donate protons in the reactions.
A catalyst is the molecule which is used to speed up the chemical reaction, not being consumed within the procedure. Acids are used as catalysts are needed for an acid catalyzed hydration.
A dehydration reaction is aeration when any organic substance loses the water molecule to form an alkene.

Answer to Problem 14.29P
False.
Explanation of Solution
The hydration of propene with water in the presence of sulfuric acid produces propanol. It is a secondary alcohol. Propanol undergoes oxidation in the presence of potassium chromate and produces propanone. There is no hydrogen atom present in propanone. So, it does not produce propanoic acid in oxidation.
Therefore, this statement is false.
Want to see more full solutions like this?
Chapter 14 Solutions
Bundle: Introduction to General, Organic and Biochemistry, 11th + OWLv2, 4 terms (24 months) Printed Access Card
- can someone draw out the reaction mechanism for this reaction showing all the curly arrows and 2. Draw the GPNA molecule and identify the phenylalanine portion. 3. Draw L-phenylalanine with the correct stereochemistryarrow_forwardWhat is the reaction mechanism for this?arrow_forwardPredict the major products of both organic reactions. Be sure to use wedge and dash bonds to show the stereochemistry of the products when it's important, for example to distinguish between two different major products. esc esc Explanation Check 2 : + + X H₁₂O + Х ง WW E R Y qab Ccaps lock shift $ P X Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility Bil T FR F18 9 G t K L Z X V B N M control opption command command T C darrow_forward
- Draw the Markovnikov product of the hydrohalogenation of this alkene. this problem. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for caps lock Explanation Check 2 W E R + X 5 HCI Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility Bil Y F G H K L ZZ X C V B N M control opption command F10 F10 command 4 BA Ar Carrow_forwardI don't understand why the amide on the top left, with the R attached to one side, doesn't get substituted with OH to form a carboxylic acid. And if only one can be substituted, why did it choose the amide it chose rather than the other amide?arrow_forwardesc Draw the Markovnikov product of the hydration of this alkene. Note for advanced students: draw only one product, and don't worry about showing any stereochemistry. Drawing dash and wedge bonds has been disabled for this problem. Explanation Check BBB + X 0 1. Hg (OAc)2, H₂O 2. Na BH 5 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibility Bl P 豆 28 2 28 N 9 W E R T Y A S aps lock G H K L Z X C V B N M T central H command #e commandarrow_forward
- C A student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. . If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. (X) This transformation can't be done in one step. + Tarrow_forwardく Predict the major products of this organic reaction. If there aren't any products, because nothing will happen, check the box under the drawing area instead. No reaction. Explanation Check OH + + ✓ 2 H₂SO 4 O xs H₂O 2 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forwardDraw the skeletal ("line") structure of 1,3-dihydroxy-2-pentanone. Click and drag to start drawing a structure. X Parrow_forward
- Predicting edict the major products of this organic reaction. If there aren't any products, because nothing will happen, check the box under the drawing area instead. + No reaction. Explanation Check HO Na O H xs H₂O 2 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Iarrow_forwardChoosing reagents and conditions for acetal formation or hydrolysis 0/5 A student proposes the transformation below in one step of an organic synthesis. There may be one or more products missing from the right-hand side, but there are no reagents missing from the left-hand side. There may also be catalysts, small inorganic reagents, and other important reaction conditions missing from the arrow. • Is the student's transformation possible? If not, check the box under the drawing area. If the student's transformation is possible, then complete the reaction by adding any missing products to the right-hand side, and adding required catalysts, inorganic reagents, or other important reaction conditions above and below the arrow. • You do not need to balance the reaction, but be sure every important organic reactant or product is shown. + This transformation can't be done in one step. 5 I H Autumn alo 值 Ar Barrow_forwardA block of copper of mass 2.00kg(cp = 0.3851 .K) and g temperature 0°C is introduced into an insulated container in which there is 1.00molH, O(g) at 100°C and 1.00 2 atm. Note that C P = 4.184. K for liquid water, and g that A H = 2260 for water. vap g Assuming all the steam is condensed to water, and that the pressure remains constant: (a) What will be the final temperature of the system? (b) What is the heat transferred from the water to the copper? (c) What is the entropy change of the water, the copper, and the total system?arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningOrganic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
- General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning




