Concept explainers
Draw the structure corresponding to each name.
a. 3-methyihexanoic acid
b. 3-hydroxy-4-methylheptanoic acid
c. p-nitrobenzoic acid
d. sodium hexanoate
e. m-ethylbenzoic acid
f. propyl decanoate
(a)
Interpretation:
The structure of 3-methylhexanoic acid should be drawn.
Concept Introduction:
The structure of organic compound is drawn in order to represent the arrangement of atoms in which they are present in a molecule.
Answer to Problem 44P
Explanation of Solution
An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H.
The IUPAC names are given to the carboxylic acid according to the following steps:
1. The parent (longest) alkane chain is identified.
2. The ending of the parent chain from alkane (-e) is changed to -oic acid for a carboxylic acid group.
3. The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.
4. Name should be written in alphabetical order and other substituents are shown by the number.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
The given name is 3-methylhexanoic acid where the parent chain is hexane that is 6 carbon atom chain having a methyl substituent at carbon-3. So, the structure of 3-methylhexanoic acid is:
(b)
Interpretation:
The structure of 3-hydroxy-4-methylheptanoic acid should be drawn.
Concept Introduction:
The structure of organic compound is drawn in order to represent the arrangement of atoms in which they are present in a molecule.
Answer to Problem 44P
Explanation of Solution
An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H.
The IUPAC names are given to the carboxylic acid according to the following steps:
1. The parent (longest) alkane chain is identified.
2. The ending of the parent chain from alkane (-e) is changed to -oic acid for a carboxylic acid group.
3. The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.
4. Name should be written in alphabetical order and other substituents are shown by the number.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
The given name is 3-hydroxy-4-methylheptanoic acid where the parent chain is heptane that is 7 carbon atom chain having a hydroxy substituent at carbon-3 and a methyl substituent at carbon-4. So, the structure of 3-hydroxy-4-methylheptanoic acid is:
(c)
Interpretation:
The structure of p-nitrobenzoic acid should be drawn.
Concept Introduction:
The structure of organic compound is drawn in order to represent the arrangement of atoms in which they are present in a molecule.
Answer to Problem 44P
Explanation of Solution
An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H.
The IUPAC names are given to the carboxylic acid according to the following steps:
1. The parent (longest) alkane chain is identified.
2. The ending of the parent chain from alkane (-e) is changed to -oic acid for a carboxylic acid group.
3. The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.
4. Name should be written in alphabetical order and other substituents are shown by the number.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
The given name is p-nitrobenzoic acid where the parent chain is benzene having a nitro substituent at carbon-4. So, the structure of p-nitrobenzoic acid is:
(d)
Interpretation:
The structure of sodium hexanoate should be drawn.
Concept Introduction:
The structure of organic compound is drawn in order to represent the arrangement of atoms in which they are present in a molecule.
Answer to Problem 44P
Explanation of Solution
An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H. When H of hydroxyl group present in carboxylic acid is replaced by an atom then it results in the formation of respective salt.
The IUPAC names are given to the carboxylic acid salt according to the following steps:
- The parent (longest) carbon chain is identified.
- The name of metal is written first from which the salt is made up of.
- The ending of the for a carboxylic acid group is changed to -oate for naming salt of carboxylic acid.
- The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.
- Name should be written in alphabetical order and other substituents are shown by the number.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
The given name is sodium hexanoate where the parent chain is hexane having 6 carbon atoms and metal is sodium. So, the structure of sodium hexanoate is:
(e)
Interpretation:
The structure of m-ethylbenzoic acid should be drawn.
Concept Introduction:
The structure of organic compound is drawn in order to represent the arrangement of atoms in which they are present in a molecule.
Answer to Problem 44P
Explanation of Solution
An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H.
The IUPAC names are given to the carboxylic acid according to the following steps:
1. The parent (longest) alkane chain is identified.
2. The ending of the parent chain from alkane (-e) is changed to -oic acid for a carboxylic acid group.
3. The numbering is of the chain is done in such a way that carbonyl carbon gets the smaller number.
4. Name should be written in alphabetical order and other substituents are shown by the number.
For number of carbons atoms chain, the prefix is given as:
Carbon-1 meth
Carbon-2 eth
Carbon-3 prop
Carbon-4 but
Carbon-5 pent
Carbon-6 hex
Carbon-7 hept
Carbon-8 oct
Carbon-9 non
Carbon-10 dec
The given name is m-ethylbenzoic acid where the parent chain is benzene having an ethyl substituent at carbon-3. So, the structure of m-ethylbenzoic acid is:
(f)
Interpretation:
The structure of propyl decanoate should be drawn.
Concept Introduction:
The structure of organic compound is drawn in order to represent the arrangement of atoms in which they are present in a molecule.
Answer to Problem 44P
Explanation of Solution
An organic compound in which carboxy functional group that is -COOH is bonded to the carbon atom is said to be a carboxylic acid. The general formula for carboxylic acid is RCOOH or RCO2H. When -H of the carboxylic acid is replaced by an alkyl or aryl group (-R') then it results in the formation of an ester having general formula RCOOR'.
The reaction which results in the formation of at least one ester along with water on heating acids with alcohols is said to be esterification.
So, in order to give the IUPAC name to the esters, the following steps are followed:
- The alkyl substituent from the alcohol is named first.
- The name of the parent chain from carboxylic acid part is replaced as carboxylate.
In order to write the common name of the esters, the common of acids are written from which the ester has been formed.
The given name is propyl decanoate where propyl name is derived from propanol and decanoate is derived from the name decanoic acid. So, the structure of propyl decanoate is:
Want to see more full solutions like this?
Chapter 17 Solutions
General, Organic, and Biological Chemistry - 4th edition
- Write the calculate the reaction quotient for the following system, if the partial pressure of all reactantsand products is 0.15 atm: NOCl (g) ⇌ NO (g) + Cl2 (g) H = 20.5 kcalarrow_forwardComplete the spectroscopy with structurearrow_forwardcould you answer the questions and draw the complete mechanismarrow_forward
- Complete the spectroscopy with structurearrow_forwardCalculate the reaction quotient for the reaction:NaOH (s) ⇌ Na+ (aq)+ OH- (aq) + 44.4 kJ [Na+] = 4.22 M [OH-] = 6.41 Marrow_forwardGiven the following concentrations for a system, calculate the value for the reaction quotient: Cl2(g)+ CS2(g) ⇌ CCl4(g)+ S2Cl2(g) Cl2 = 31.1 atm CS2 = 91.2 atm CCl4 = 2.12 atm S2Cl2 = 10.4 atmarrow_forward
- Match each chemical or item with the proper disposal or cleanup mwthod, Not all disposal and cleanup methods will be labeled. Metal sheets C, calcium, choroide solutions part A, damp metal pieces Part B, volumetric flask part A. a.Return to correct lables”drying out breaker. Place used items in the drawer.: Rinse with deionized water, dry as best you can, return to instructor. Return used material to the instructor.: Pour down the sink with planty of running water.: f.Pour into aqueous waste container. g.Places used items in garbage.arrow_forwardWrite the equilibrium constant expression for the following reaction: HNO2(aq) + H2O(l) ⇌ H3O+(aq) + NO2-(aq)arrow_forwardWrite the reaction quotient for: Pb2+(aq) + 2 Cl- (aq) ⇌ PbCl2(s)arrow_forward
- Write the equilibrium constant expression for the following system at equilibrium: I2 (g) ⇌ 2 I (g)arrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forwardWe learned four factors (ARIO) for comparing the relative acidity of compounds. When two of these factors are in competition, the order of priority is the order in which these factors were covered ("atom" being the most important factor and "orbital" being the least important). However, we also mentioned that there are exceptions to this order of priority. Compare the two compounds and identify the exception. OH PK-4.75 SH PK-10.6 5. "Resonance" is more important than "atom" because the conjugate base of first compound is more stable than the second. "Atom" is more important than "resonance" because the conjugate base of first compound is more stable than the second. "Resonance" is more important than "atom" because the conjugate base of second compound is more stable than the first. "Atom" is more important than "resonance" because the conjugate base of second compound is more stable than the first.arrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY