(a)
Interpretation:
The structural formula for
Concept Introduction:
In
In organic chemistry, reduction reaction is referred to the number
Alcohols undergo
Aldehyde undergoes oxidation to give carboxylic acid as the product while ketone does not undergo oxidation reaction.
(a)
Answer to Problem 16.46EP
The structural formula of the expected product is,
Explanation of Solution
Aldehyde on oxidation gives carboxylic acid as the product. The general scheme can be represented as shown below,
Given substance is,
The given compound is propanal and it is an aldehyde. Propanal on oxidation gives propanoic acid as the product. The complete scheme can be represented as shown below,
The carboxylic acid that is formed on oxidation of the given substance is propanoic acid. The structural formula of propanoic acid is given below,
Structural formula of the carboxylic acid formed by the oxidation of given substance is drawn.
(b)
Interpretation:
The structural formula for carboxylic acid that is expected to be formed on oxidation of the given substance has to be drawn.
Concept Introduction:
In organic chemistry, oxidation reaction is referred to the number
In organic chemistry, reduction reaction is referred to the number
Alcohols undergo oxidation reaction and reduction reaction. This depends upon the number of hydrogen atoms that is bonded to the alpha carbon atom. Primary and secondary alcohol undergoes oxidation reaction while tertiary alcohol does not undergo oxidation reaction. Primary alcohols undergo oxidation to give aldehyde and carboxylic acid as product. Secondary alcohol undergoes oxidation to give ketone as the product.
Aldehyde undergoes oxidation to give carboxylic acid as the product while ketone does not undergo oxidation reaction.
Aromatic carboxylic acids are prepared from alkyl substituted benzenes.
(b)
Answer to Problem 16.46EP
The structural formula of the expected product is,
Explanation of Solution
Primary alcohol on oxidation gives aldehyde as intermediate product. This on further oxidation gives carboxylic acid as the product. The general scheme can be represented as shown below,
Given substance is,
This is a primary alcohol. The given compound is propanol. Propanol on oxidation gives propanal as the intermediate product. The formed propanal on oxidation gives propanoic acid as the product. The complete scheme can be represented as shown below,
The carboxylic acid that is formed on oxidation of the given substance is propanoic acid. The structural formula of propanoic acid is given below,
Structural formula of the carboxylic acid formed by the oxidation of given substance is drawn.
(c)
Interpretation:
The structural formula for carboxylic acid that is expected to be formed on oxidation of the given substance has to be drawn.
Concept Introduction:
In organic chemistry, oxidation reaction is referred to the number
In organic chemistry, reduction reaction is referred to the number
Alcohols undergo oxidation reaction and reduction reaction. This depends upon the number of hydrogen atoms that is bonded to the alpha carbon atom. Primary and secondary alcohol undergoes oxidation reaction while tertiary alcohol does not undergo oxidation reaction. Primary alcohols undergo oxidation to give aldehyde and carboxylic acid as product. Secondary alcohol undergoes oxidation to give ketone as the product.
Aldehyde undergoes oxidation to give carboxylic acid as the product while ketone does not undergo oxidation reaction.
Aromatic carboxylic acids are prepared from alkyl substituted benzenes.
(c)
Answer to Problem 16.46EP
The structural formula of the expected product is,
Explanation of Solution
Aldehyde on oxidation gives carboxylic acid as the product. The general scheme can be represented as shown below,
Given substance is,
The given compound is 2,3-dimethylbutanal and it is an aldehyde. 2,3-dimethylbutanal on oxidation gives 2,3-dimethylbutanoic acid as the product. The complete scheme can be represented as shown below,
The carboxylic acid that is formed on oxidation of the given substance is 2,3-dimethylbutanoic acid. The structural formula of 2,3-dimethylbutanoic acid is given below,
Structural formula of the carboxylic acid formed by the oxidation of given substance is drawn.
(d)
Interpretation:
The structural formula for carboxylic acid that is expected to be formed on oxidation of the given substance has to be drawn.
Concept Introduction:
In organic chemistry, oxidation reaction is referred to the number
In organic chemistry, reduction reaction is referred to the number
Alcohols undergo oxidation reaction and reduction reaction. This depends upon the number of hydrogen atoms that is bonded to the alpha carbon atom. Primary and secondary alcohol undergoes oxidation reaction while tertiary alcohol does not undergo oxidation reaction. Primary alcohols undergo oxidation to give aldehyde and carboxylic acid as product. Secondary alcohol undergoes oxidation to give ketone as the product.
Aldehyde undergoes oxidation to give carboxylic acid as the product while ketone does not undergo oxidation reaction.
Aromatic carboxylic acids are prepared from alkyl substituted benzenes.
(d)
Answer to Problem 16.46EP
The structural formula of the expected product is,
Explanation of Solution
Given substance is,
Oxidation of the alkyl side chain in a benzene derivative leads to the formation of aromatic acids. All the carbon atoms in alkyl group are lost except the one that is attached to the ring. The one carbon that is attached to the ring becomes a part of carboxyl
The product formed is benzoic acid.
Structural formula of the carboxylic acid formed by the oxidation of given substance is drawn.
Want to see more full solutions like this?
Chapter 16 Solutions
General, Organic, and Biological Chemistry
- Don't used Ai solutionarrow_forward5. A solution of sucrose is fermented in a vessel until the evolution of CO2 ceases. Then, the product solution is analyzed and found to contain, 45% ethanol; 5% acetic acid; and 15% glycerin by weight. If the original charge is 500 kg, evaluate; e. The ratio of sucrose to water in the original charge (wt/wt). f. Moles of CO2 evolved. g. Maximum possible amount of ethanol that could be formed. h. Conversion efficiency. i. Per cent excess of excess reactant. Reactions: Inversion reaction: C12H22O11 + H2O →2C6H12O6 Fermentation reaction: C6H12O6 →→2C2H5OH + 2CO2 Formation of acetic acid and glycerin: C6H12O6 + C2H5OH + H₂O→ CH3COOH + 2C3H8O3arrow_forwardShow work. don't give Ai generated solution. How many carbons and hydrogens are in the structure?arrow_forward
- 13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B 2°C. +2°C. cleavage Bond A •CH3 + 26.← Cleavage 2°C. + Bond C +3°C• CH3 2C Cleavage E 2°C. 26. weakest bond Intact molecule Strongest 3°C 20. Gund Largest argest a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. C Weakest bond A Produces Most Bond Strongest Bond Strongest Gund produces least stable radicals Weakest Stable radical b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. 13°C. formed in bound C cleavage ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. • CH3 methyl radical Formed in Gund A Cleavage c.…arrow_forwardBr. COOH Br, FCH COOH E FeBr ASOCI B NH (CH,CO),OD Br₂ 2 C alcKOHarrow_forwardFind A to F (all)arrow_forward
- Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage LearningChemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
- General Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage Learning