![General, Organic, and Biological Chemistry - 4th edition](https://www.bartleby.com/isbn_cover_images/9781259883989/9781259883989_largeCoverImage.gif)
Concept explainers
(a)
Interpretation:
The oxidized product of the following alcohol when oxidized with
Concept Introduction:
A
In a chemical reaction, the substance which is involved in conversion is said to be reactant whereas the newly formed substance is known as a product. Both reactants and products must be separated by an arrow.
The oxidation reaction is the reaction that involves the addition of O atom in the presence of certain oxidizing agents such as
![Check Mark](/static/check-mark.png)
Answer to Problem 64P
Explanation of Solution
To get the oxidized product of any alcohol, three steps must be followed:
- Locate the C atom in the parent chain that is bonded with −OH group.
- Convert that C atom to carbonyl C atom or
carboxylic acid as it is overall removal of H atoms. - Primary alcohols are oxidized to
aldehyde which further oxidized to a carboxylic acid. - Secondary alcohols are oxidized to
ketone (R2CO). - Tertiary alcohols are not oxidized as they do not have H atom on the C with the −OH group.
Hence, the oxidized of 2-methylcyclopnetanol will form 2-methylcyclopentanone molecule as 2-methylcyclopnetanol is a secondary alcohol.
(b)
Interpretation:
The oxidized product of the following alcohol when oxidized with
Concept Introduction:
A chemical reaction is the symbolic representation of the conversion of substances to new substances.
In a chemical reaction, the substance which is involved in conversion is said to be reactant, whereas the newly formed substance is known as a product. Both reactants and products must be separated by an arrow.
The oxidation reaction is the reaction that involves the addition of O atom in the presence of certain oxidizing agents such as
![Check Mark](/static/check-mark.png)
Answer to Problem 64P
Explanation of Solution
To get the oxidized product of any alcohol, three steps must be followed:
- Locate the C atom in the parent chain that is bonded with −OH group.
- Convert that C atom to carbonyl C atom or carboxylic acid as it is overall removal of H atoms.
- Primary alcohols are oxidized to aldehyde which further oxidized to the carboxylic acid.
- Secondary alcohols are oxidized to ketone (R2CO).
- Tertiary alcohols are not oxidized as they do not have H atom on the C with the −OH group.
Hence, the oxidized of 1-decanol will form decanoic acid molecule as 1-decanol is a primary alcohol.
(c)
Interpretation:
The oxidized product of following alcohol when oxidized with
Concept Introduction:
A chemical reaction is the symbolic representation of the conversion of substances to new substances.
In a chemical reaction; the substance which is involved in conversion is said to be reactant whereas the newly formed substance is known as a product. Both reactants and products must be separated by an arrow.
The oxidation reaction is the reaction that involves the addition of O atom in the presence of certain oxidizing agents such as
![Check Mark](/static/check-mark.png)
Answer to Problem 64P
Explanation of Solution
To get the oxidized product of any alcohol, three steps must be followed:
- Locate the C atom in the parent chain that is bonded with −OH group.
- Convert that C atom to carbonyl C atom or carboxylic acid as it is overall removal of H atoms.
- Primary alcohols are oxidized to aldehyde which further oxidized to the carboxylic acid.
- Secondary alcohols are oxidized to a ketone (R2CO).
- Tertiary alcohols are not oxidized as they do not have H atom on the C with the −OH group.
Hence, the oxidized of cyclopentylmethanol will form cyclopentanecarboxylic acid molecule as cyclopentylmethanol is a primary alcohol.
(d)
Interpretation:
The oxidized product of following alcohol when oxidized with
Concept Introduction:
A chemical reaction is the symbolic representation of the conversion of substances to new substances.
In a chemical reaction; the substance which is involved in conversion is said to be reactant whereas the newly formed substance is known as a product. Both reactants and products must be separated by an arrow.
Oxidation reaction is the reaction that involves the addition of O atom in the presence of certain oxidizing agents such as
![Check Mark](/static/check-mark.png)
Answer to Problem 64P
2-ethyl-3-pentanol cannot oxidize as it is a tertiary alcohol.
Explanation of Solution
To get the oxidized product of any alcohol, three steps must be followed;
- Locate the C atom in the parent chain that is bonded with −OH group.
- Convert that C atom to carbonyl C atom or carboxylic acid as it is the overall removal of H atoms.
- Primary alcohols are oxidized to aldehyde which further oxidized to the carboxylic acid.
- Secondary alcohol is oxidized to a ketone (R2CO).
- Tertiary alcohols are not oxidized as they do not have H atom on the C with the −OH group.
Hence 2-ethyl-3-pentanol cannot oxidize as it is a tertiary alcohol.
Want to see more full solutions like this?
Chapter 14 Solutions
General, Organic, and Biological Chemistry - 4th edition
- Please correct answer and don't use hand rating and don't use Ai solutionarrow_forwardHow would you distinguish the following compounds from each other using IR only (GRADED)? NH2 HN VS کر A B VS N. Carrow_forwardQ4: Draw the mirror image of the following molecules. Are the molecules chiral? C/ F CI CI CH3 CI CH3 CI CH3 CH 3 |||||... CH3arrow_forward
- Q6: Monochlorination of methylcyclopentane can result in several products. When the chlorination occurs at the C2 position, how many stereoisomers are formed? If more than one is formed, are they generated in equal or unequal amounts? 2arrow_forwardShow work. Don't give Ai generated solutionarrow_forwardPlease correct answer and don't use hand ratingarrow_forward
- Introductory Chemistry: A FoundationChemistryISBN:9781285199030Author:Steven S. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285199030/9781285199030_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305080485/9781305080485_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780534420123/9780534420123_smallCoverImage.gif)