
(a)
Interpretation:
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of esters of carboxylic acids:
The acyl group bonded to
The naming of an ester of a
(a)

Explanation of Solution
The name of the compound is given below:
Dimethyl carbonate
From the name, it is clear that two methyl groups are attached to oxygen atoms in the compound and the parent ester group is carbonate.
Thus, the structure of the compound is given below:
(b)
Interpretation:
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of nitriles:
The numbering 1 can be given to the nitrile carbon atom and add nitrile to end of the
(b)

Explanation of Solution
The name of the compound is given below:
The functional group is nitrile and benzene ring is attached to it.
Thus, the structure of the compound is given below:
Benzo nitrile
(c)
Interpretation:
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of esters of carboxylic acids:
The acyl group bonded to
The naming of an ester of a carboxylic acid is done by naming alkyl or aryl group bonded to oxygen first followed by the name of the acid in which the suffix –ic acid is replaced by the suffix –ate.
(c)

Explanation of Solution
The name of the compound is given below:
Isopropyl-3-methylhexanoate
The alkyl group attached on oxygen atom is the isopropyl group and the parent chain is the methylhexanoate.
Thus, the structure of the compound is given below:
(d)
Interpretation:
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of esters of carboxylic acids:
The acyl group bonded to
The naming of an ester of a carboxylic acid is done by naming alkyl or aryl group bonded to oxygen first followed by the name of the acid in which the suffix –ic acid is replaced by the suffix –ate.
(d)

Explanation of Solution
The name of the compound is given below:
Diethyl oxalate
From the name, it is clear that two ethyl groups are attached to oxygen atoms in the compound and the parent ester group is oxalate.
Thus, the structure of the compound is given below:
(e)
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of esters of carboxylic acids:
The acyl group bonded to
The naming of an ester of a carboxylic acid is done by naming alkyl or aryl group bonded to oxygen first followed by the name of the acid in which the suffix –ic acid is replaced by the suffix –ate.
(e)

Explanation of Solution
The name of the compound is given below:
Ethyl (Z)-2-pentenoate
The alkyl group attached on oxygen atom is the ethyl group and the parent chain is the pentenoate. The double bond is having E configuration.
Thus, the structure of the compound is given below:
(f)
Interpretation:
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of anhydrides:
The nomenclature of anhydride involves replacement of the word acid with anhydride. In the case of mixed anhydrides, both acids should be named.
(f)

Explanation of Solution
The name of the compound is given below:
Butanoic anhydride
From the butanoic acid, acid part can be replaced with an anhydride group.
(g)
Interpretation:
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of amides and imides:
The acyl group bonded to a nitrogen atom is the functional group of an amide.
The naming of an amide can be done by giving the suffix –oic acid from the IUPAC name of the parent acid and adding –amide.
The location of the alkyl or aryl group attached on nitrogen atom in an amide is indicated by ‘N-‘
The indication “ N,N-di-“ is used for two identical alkyl or aryl groups on nitrogen atom
(g)

Explanation of Solution
The name of the compound is given below:
Dodecanamide:
The functional group is amide and the acyl group attached is the dodecane group.
Thus, the structure of the compound is given below:
(h)
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of esters of carboxylic acids:
The acyl group bonded to
The naming of an ester of a carboxylic acid is done by naming alkyl or aryl group bonded to oxygen first followed by the name of the acid in which the suffix –ic acid is replaced by the suffix –ate.
(h)

Explanation of Solution
The name of the compound is given below:
Ethyl-3-hydroxybutanoate
The alkyl group attached on oxygen atom is the ethyl group and the parent chain is the butanoate and a hydroxyl group is present in the third position.
Thus, the structure of the compound is given below:
(i)
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of acid chlorides:
The nomenclture of acid chlorides can be done by replacing –oic acid with –oyl chloride.
(i)

Explanation of Solution
The name of the compound is given below:
Octanoyl chloride
The acid group from the octanoic acid will be replaced by acid chloride group.
Thus, the structure of the compound is given below:
(j)
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of esters of carboxylic acids:
The acyl group bonded to
The naming of an ester of a carboxylic acid is done by naming alkyl or aryl group bonded to oxygen first followed by the name of the acid in which the suffix –ic acid is replaced by the suffix –ate.
(j)

Explanation of Solution
The name of the compound is given below:
Diethyl cis-1,2-cyclohexanedicarboxylate
The alkyl group attached on oxygen atom are two ethyl groups and the parent chain is the dicarboxylate and a cyclohecxane group is present in the 1,2 position.
Thus, the structure of the compound is given below:
(k)
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of acid chlorides:
The nomenclture of acid chlorides can be done by replacing –oic acid with –oyl chloride.
(k)

Explanation of Solution
The name of the compound is given below:
Methanesulfonyl chloride
The acid group from the methanesulfonic acid will be replaced by acid chloride group.
Thus, the structure of the compound is given below:
(l)
The structural formula for the given compound has to be drawn.
Concept introduction:
Nomenclature of acid chlorides:
The nomenclture of acid chlorides can be done by replacing –oic acid with –oyl chloride.
(l)

Explanation of Solution
The name of the compound is given below:
p-Toluenesulfonyl chloride
The acid group from the p-toluenesulfonic acid will be replaced by acid chloride group.
Thus, the structure of the compound is given below:
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Chapter 18 Solutions
Organic Chemistry, Loose-leaf Version
- Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electrons-pushing arrows for the following reaction or mechanistic step(s).arrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. I I I H Select to Add Arrows HCI, CH3CH2OHarrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and the follow the arrows to draw the intermediate and product in this reaction or mechanistic step(s).arrow_forward
- Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to draw the intermediates and product of the following reaction or mechanistic step(s).arrow_forwardCurved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the arrows to draw the intermediate and the product in this reaction or mechanistic step(s).arrow_forwardLook at the following pairs of structures carefully to identify them as representing a) completely different compounds, b) compounds that are structural isomers of each other, c) compounds that are geometric isomers of each other, d) conformers of the same compound (part of structure rotated around a single bond) or e) the same structure.arrow_forward
- Given 10.0 g of NaOH, what volume of a 0.100 M solution of H2SO4 would be required to exactly react all the NaOH?arrow_forward3.50 g of Li are combined with 3.50 g of N2. What is the maximum mass of Li3N that can be produced? 6 Li + N2 ---> 2 Li3Narrow_forward3.50 g of Li are combined with 3.50 g of N2. What is the maximum mass of Li3N that can be produced? 6 Li + N2 ---> 2 Li3Narrow_forward
- Concentration Trial1 Concentration of iodide solution (mA) 255.8 Concentration of thiosulfate solution (mM) 47.0 Concentration of hydrogen peroxide solution (mM) 110.1 Temperature of iodide solution ('C) 25.0 Volume of iodide solution (1) used (mL) 10.0 Volume of thiosulfate solution (5:03) used (mL) Volume of DI water used (mL) Volume of hydrogen peroxide solution (H₂O₂) used (mL) 1.0 2.5 7.5 Time (s) 16.9 Dark blue Observations Initial concentration of iodide in reaction (mA) Initial concentration of thiosulfate in reaction (mA) Initial concentration of hydrogen peroxide in reaction (mA) Initial Rate (mA's)arrow_forwardDraw the condensed or line-angle structure for an alkene with the formula C5H10. Note: Avoid selecting cis-/trans- isomers in this exercise. Draw two additional condensed or line-angle structures for alkenes with the formula C5H10. Record the name of the isomers in Data Table 1. Repeat steps for 2 cyclic isomers of C5H10arrow_forwardExplain why the following names of the structures are incorrect. CH2CH3 CH3-C=CH-CH2-CH3 a. 2-ethyl-2-pentene CH3 | CH3-CH-CH2-CH=CH2 b. 2-methyl-4-pentenearrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
