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(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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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)
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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
- Problem 3-42 Consider 2-methylbutane (isopentane). Sighting along the C2-C3 bond: (a) Draw a Newman projection of the most stable conformation. (b) Draw a Newman projection of the least stable conformation. Problem 3-44 Construct a qualitative potential-energy diagram for rotation about the C-C bond of 1,2-dibromoethane. Which conformation would you expect to be most stable? Label the anti and gauche conformations of 1,2- dibromoethane. Problem 3-45 Which conformation of 1,2-dibromoethane (Problem 3-44) would you expect to have the largest dipole moment? The observed dipole moment of 1,2-dibromoethane is µ = 1.0 D. What does this tell you about the actual conformation of the molecule?arrow_forwardGas Law Studies 1. Mass of zinc Determination of 0.899 2) Moles of zinc 0.01361 mol 3.) Moles of hydrogen 00? ← I was told to calculate this number from mole of zinc. 350m So does that mean it will be 0.01361 mol too? 4 Volume of water collected (mL) 5) VL of water collected (Liters) 0.350 L 6) Temp of water collected (°C) 7) Temp of water collected (°K) 8) Atmospheric pressure (mm) 9) Vapor pressure of water (mm) 10) Corrected pressure of hydrogen 20% 29°C 764.0mm Hg (mm) 17.5mm 11) Corrected pressure of hydrogen (atm) 12) Experimentally calculated value of 19 13. Literature value of R 14) % Error 15) Suggest reasons for the % error (#14)arrow_forwardNo wedge or dashes. Do proper structure. Provide steps and explanation.arrow_forward
- 10 Question (1 point) Draw curved arrow notation to indicate the proton transfer between NaOH and CH3CO₂H. 2nd attempt :0- H See Periodic Table See Hint Draw the products of the proton transfer reaction. Don't add a + sign between the products.arrow_forwardProvide steps and explanation please.arrow_forwardProvide steps to name and label for understanding.arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
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