
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

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

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

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

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.
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Chapter 14 Solutions
Loose Leaf for General, Organic and Biological Chemistry with Connect 2 Year Access Card
- Predict the product of this organic reaction: IZ + HO i P+H₂O Specifically, in the drawing area below draw the skeletal ("line") structure of P. If there is no reasonable possibility for P, check the No answer box under the drawing area. No Answer Click and drag to start drawing a structure. ☐ :arrow_forwardPredict the products of this organic reaction: 0 O ----- A + KOH ? CH3-CH2-C-O-CH2-C-CH3 Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No reaction Click anywhere to draw the first atom of your structure. X ⑤ èarrow_forwardPredict the products of this organic reaction: O CH3 + H2O + HCI A A? CH3-CH2-C-N-CH3 Specifically, in the drawing area below draw the condensed structure of the product, or products, of this reaction. If there's more than one product, draw them in any arrangement you like, so long as they aren't touching. If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No Reaction Click anywhere to draw the first atom of your structure.arrow_forward
- What is the missing reactant in this organic reaction? R+ HO-C-CH2-CH3 0= CH3 CH3 —CH, C−NH—CH CH3 + H₂O Specifically, in the drawing area below draw the condensed structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. Note for advanced students: you may assume no products other than those shown above are formed. No Answer Click anywhere to draw the first atom of your structure. €arrow_forward个 CHEM&131 9267 - $25 - Intro to Mail - Hutchison, Allison (Student x Aktiv Learnin https://app.aktiv.com Draw the product of the reaction shown below. Ignore inorganic byproducts. + Na2Cr2O7 Acetone, H2SO4 Type here to search Dryng OH W Prarrow_forwardPredict the products of this organic reaction: OH + NaOH A? Specifically, in the drawing area below draw the skeletal ("line") structure of the product, or products, of this reaction. (If there's more than one product, draw them in any arrangement you like, so long as they aren't touching.) If there aren't any products because this reaction won't happen, check the No reaction box under the drawing area. No reaction Click and drag to start drawing a structure. ✓ Sarrow_forward
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- Predict the major organic products of the reaction below and draw them on right side of the arrow. If there will be no significant reaction, check the box below the drawing area instead. C Cl CH, OH There will be no significant reaction. + pyridine G Click and drag to start drawing a structure.arrow_forwardWhat is the missing reactant in this organic reaction? H R+ H2O Δ OH 0= CH3-CH-O-CH3 + CH3-C-OH Specifically, in the drawing area below draw the condensed structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. No Answer Click anywhere to draw the first atom of your structure. dyarrow_forwardYou are trying to determine whether the following organic reaction can be done in a single synthesis step. If so, add any missing reagents or conditions in the drawing area below. If it isn't possible to do this reaction in a single synthesis step, check the box below the drawing area instead. Note for advanced students: if you have a choice of reagents to add, you should choose the least reactive and most economical reagents possible. Cl It isn't possible to do this reaction in a single synthesis step. + T OHarrow_forward
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