(a)
Interpretation: The structures of the final products formed in the following reactions are to be stated.
Concept introduction: Organic compounds are synthesized through organic reactions. The different types of reactions in
To determine: The structure of
(a)
Explanation of Solution
Explanation
The structure of
The structure of
Figure 1
The given reactant is
(b)
Interpretation: The structures of the final products formed in the following reactions are to be stated.
Concept introduction: Organic compounds are synthesized through organic reactions. The different types of reactions in organic chemistry are elimination reaction, substitution reaction, addition reactions and many more. Addition reactions are takes place when two or more reactants combine to form a single product. Elimination reactions occur when a reactant broke down into two or more products and the substitution reactions takes place by an exchange in the reactants.
To determine: The structure of
(b)
Explanation of Solution
Explanation
The structure of
The structure of
Figure 2
The given reactant reacts with water to form tertiary alcohol as the major product. As tertiary alcohols are formed by the dehydration of
(c)
Interpretation: The structures of the final products formed in the following reactions are to be stated.
Concept introduction: Organic compounds are synthesized through organic reactions. The different types of reactions in organic chemistry are elimination reaction, substitution reaction, addition reactions and many more. Addition reactions are takes place when two or more reactants combine to form a single product. Elimination reactions occur when a reactant broke down into two or more products and the substitution reactions takes place by an exchange in the reactants.
To determine: The two possible structures of
(c)
Explanation of Solution
Explanation
The two possible structures of
The two possible structures of
Figure 3
The given chemical formula is
(d)
Interpretation: The structures of the final products formed in the following reactions are to be stated.
Concept introduction: Organic compounds are synthesized through organic reactions. The different types of reactions in organic chemistry are elimination reaction, substitution reaction, addition reactions and many more. Addition reactions are takes place when two or more reactants combine to form a single product. Elimination reactions occur when a reactant broke down into two or more products and the substitution reactions takes place by an exchange in the reactants.
To determine: The structure of hydrocarbon reacted with
(d)
Explanation of Solution
Explanation
The structure of hydrocarbon is shown in Figure 4.
The structure of hydrocarbon is,
Figure 4
The given hydrocarbon reacts with water which is further oxidized to give acetone. Therefore, the given hydrocarbon should be alkene which is propene as the major product is
(e)
Interpretation: The structures of the final products formed in the following reactions are to be stated.
Concept introduction: Organic compounds are synthesized through organic reactions. The different types of reactions in organic chemistry are elimination reaction, substitution reaction, addition reactions and many more. Addition reactions are takes place when two or more reactants combine to form a single product. Elimination reactions occur when a reactant broke down into two or more products and the substitution reactions takes place by an exchange in the reactants.
To determine: The possible structures for
(e)
Explanation of Solution
Explanation
The first possible structure for
The first possible structure for
Figure 5
The major product for this reaction is
The second possible structure for
The second possible structure for
Figure 6
The isomer for the given reactant
The third possible structure for
The third possible structure for
Figure 7
The isomer for the given reactant
The fourth possible structure for
The fourth possible structure for
Figure 8
The isomer for the given reactant
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Chapter 21 Solutions
Chemistry: An Atoms First Approach
- Alcohols are very useful starting materials for the production of many different compounds. The following conversions, starting with 1-butanol, can be carried out in two or more steps. Show the steps (reactants/catalysts) you would follow to carry out the conversions, drawing the formula for the organic product in each step. For each step, a major product must be produced. (See Exercise 62.) (Hint: In the presence of H+, an alcohol is converted into an alkene and water. This is the exact reverse of the reaction of adding water to an alkene to form an alcohol.) a. 1-butanol butane b. 1-butanol 2-butanonearrow_forwardAlcohols A, B and C all have the composition C4H 100. Molecules of alcohol A contain a branched carbon chain and can be oxidized to an aldehyde; molecules of alcohol B contain a linear carbon chain and can be oxidized to a ketone; and molecules of alcohol C can be oxidized to neither an aldehyde nor a ketone. Write the Lewis structures of these molecules.arrow_forwardDistinguish between isomerism and resonance. Distinguish between structural and geometric isomerism. When writing the various structural isomers, the most difficult task is identifying which are different isomers and which are identical to a previously written structurethat is, which are compounds that differ only by the rotation of a carbon single bond. How do you distinguish between structural isomers and those that are identical? Alkenes and cycloalkanes are structural isomers of each other. Give an example of each using C4H8. Another common feature of alkenes and cycloalkanes is that both have restricted rotation about one or more bonds in the compound, so both can exhibit cis- trans isomerism. What is required for an alkene or cycloalkane to exhibit cis-trans isomerism? Explain the difference between cis and trans isomers. Alcohols and ethers are structural isomers of each other, as are aldehydes and ketones. Give an example of each to illustrate. Which functional group in Table 21-4 can be structural isomers of carboxylic acids? What is optical isomerism? What do you look for to determine whether an organic compound exhibits optical isomerism? 1-Bromo-1-chloroethane is optically active whereas 1-bromo-2-chloroethane is not optically active. Explain.arrow_forward
- I need help, it is asking what alcohols can be used to produce the products.arrow_forwardD. Ethene 73. The reagent KMN04 is used to completely oxidize acetylene. What is an expected property of the last oxidized form of acetylene? A. It will be soluble in hexane. B. It will exhibit acidic properties. C. It will form precipitate with NaCl. D. It will ionize into carbon and hydrogen. 74. As the molecular weight of alkenes increases, the boiling points also increase. Which of the following factors is best associated to this trend? A. Geometric isomerism B. Surface area C. Dipole interaction D. Structural isomerism 75. Which among the following compounds has the most electronegative carbon in its structure? A. Butyne B. Benzene C. Cyclobutane D. Benzaldehyde 76. Identify the SYSTEMATIC name of the molecule that is illustrated in this item, A. 2,4,6-trinitrotoluene B. 2-methyl-1,3,5-nitrobenzene C. 1-methyl-1,3,5-trinitrobenzene D. 1,3,5-trinitrotoluene CH3 NO2 O2N NO2 77 Identify the SYSTEMATIC name of the molecule that is illustrated in this item. A 1-methylbenzenesulfonic…arrow_forward. The following chemical reactants produce the ester ethylethanoate (C4H8O2):C2H6O + CH3COOHWhat type of reaction occurs to make ethyl ethanoate?a. condensationb. hydrolysisc. combustiond. acid-base reactionarrow_forward
- Write the structure of the product formed in the following oxidation-reduction reactions. Label the functional group in the reactant that changes, and identify the new functional group in the product. If the functional group is an alcohol, identify the type of alcohol. If there is no reaction, state so. 54 Ac a. H. ОНН Н [O] Н-С-С—С-С-Н of H. ННН b. НННС 84 Н-С-С-С--С--Н ННН C. НННН [0] form НО-С-С-С-С-Н H HH H Hd. HO [H] pertortm e. [0] ОН কনarrow_forwardCa(OH)2 4. Cr(OH)3 27. Which type of reaction is represented by the equation below? Note: n and n are very large numbers equal to about 2000. <)-(H) 1. esterification 2. fermentation 3. saponification 4. polymerization Which functional group, when attached to a chain of carbon atoms. perties of an aldehyde? istisarrow_forward13. Ethylethanoate and butanoic acid can be classified as A. positional isomers B. chain isomers C. functional isomers D. stereoisomers 14. Which of the following pairs are positional isomers A. trans-1,4-dichlorocyclohexane, cis-1,3-dichlorocyclopentane B. trans 1,4-dichlorocyclohexane, cis-1,4-dichlorocyclohexane C. 2-pentanol, Cyclopentanol D. 1,2-cycohexanediol, 1,3-cycohexanediol 15. Which of the following compounds will have zero dipole moment? A. cis-1,2-dibromoethylene B. 1,1-dibromoethylene C. trans-1,2-dibromoethylene D. all of these 16. Which of the following is not aromatic: A. cyclopentadienyl cation B. cyclopentadienyl anion C. Cyclopropenyl cation D. Cycloheptatrienyl cation 17. Which of the following compounds containing lone pair has the least tendency to donate its electrons? A. the lone pair in pyridine B. the lone pair in furan C. the lone pair in pyrole D. the lone pair in thiophenearrow_forward
- Which of the following alcohols can be oxidized to a carboxylic acid? Name the carboxylic acid produced. Forthose alcohols that cannot be oxidized to a carboxylic acid,name the final product.a. Ethanol c. 1-Propanolb. 2-Propanol d. 3-Pentanolarrow_forward8. Which statement regarding oxidation and reduction is false? A. An alkyne is more oxidized than alkene. B. A ketone is more oxidized than an ester C. A carboxylic acid is more oxidized than an alcohol D. Fe³+ is more oxidized than Fe²+ E. All of the above statements are true.arrow_forward1. Dehydration: 2. Oxidation: This is a reaction where an alcohol loses a water molecule to form an alkene. For example, when ethanol is treated with an acidic catalyst, such as sulfuric acid, it undergoes dehydration to form ethene (CH2=CH2) and water. ALCOHOLS In this reaction, an alcohol is converted to either a carbonyl compound or a carboxylic acid. 3. Esterification: Types of Reaction (s) For example, primary alcohols can be oxidized to aldehydes or carboxylic acids, while secondary alcohols can be oxidized to ketones. Tertiary alcohols are usually not affected by oxidations 4. Substitution: The conversion of an alcohol and a carboxylic acid to an ester and water, in the presence of an acid catalyst. The reaction between methanol and acetic acid to form methyl acetate: CH3OH + CH3COOH CH3COOCH3 + H2O Click to add speaker notes ME Substitution reactions in organic chemistry involve the replacement of one atom or group of atoms with another atom or group of atoms in a molecule. 1.…arrow_forward
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