(a)
Interpretation:
The systematic name and common name for the given set of molecules should be identified.
Concept introduction:
Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…
Suffix represents the substituent present in the molecule. It can be any
Root word represents the longest continuous carbon skeleton present in the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.
Common Name: It is quiet opposite to systematic name which is used for branched groups.
Chirality: It refers to a Carbon atom in a molecule that contains four different substituents.
Enantiomers: they are chiral molecules whose mirror images are not superimposable.
R and S nomenclature: it is used to assign the molecule using CIP rules.
The CIP rules are as follows:
Select the chiral carbon and assign the numbers according to the decreasing
If the numbering follows clockwise direction then the molecule is termed as R and if it follows anti-clockwise direction then molecule is termed as S.
(a)
Answer to Problem 47PP
Systematic name: 2-choloropropane and the common name: iso-propylchloride.
Explanation of Solution
To identify: The systematic name and the common name for the given molecules.
Find the longest carbon chain in the given molecule and assign number accordingly so that the substituent in the molecule present in the least
The given molecule is drawn. In the given molecule the parent carbon skeleton is 3 membered linear chain and the root name for this molecule is propane.
The carbon chain should be numbered such that the substituent present in the molecule should be given the least number in the carbon chain.
The substituent present in the molecule should be termed as chloro which is the prefix part should be written along with the number to where it is attached.
Therefore the systematic name is 2-choloropropane.
Find the common name for the given molecule by considering the position of carbon atoms attached.
The given molecule contains two methyl groups bonded to same carbon atom in the second position and also it consists one Choloro group which should be suffixed using ide.
Therefore the common name for the given molecule is iso-propylchloride.
Conclusion
The systematic name and the common name for the given molecules are identified by using the atoms attached to the respective carbon with the help of using
(b)
Interpretation:
The systematic name and common name for the given set of molecules should be identified.
Concept introduction:
Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…
Suffix represents the substituent present in the molecule. It can be any alkene, alkyne, alcohol, carboxylic acid, alcohol etc...
Root word represents the longest continuous carbon skeleton present in the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.
Common Name: It is quiet opposite to systematic name which is used for branched groups.
Chirality: It refers to a Carbon atom in a molecule that contains four different substituents.
Enantiomers: they are chiral molecules whose mirror images are not superimposable.
R and S nomenclature: it is used to assign the molecule using CIP rules.
The CIP rules are as follows:
Select the chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it.
If the numbering follows clockwise direction then the molecule is termed as R and if it follows anti-clockwise direction then molecule is termed as S.
(b)
Answer to Problem 47PP
Systematic name: 2-bromo-2-methylpropane and the common name: tert-butylbromide.
Explanation of Solution
Find the longest carbon chain in the given molecule and number it accordingly so that the substituent in the molecule present in the least numbered carbon atoms.
The given molecule is drawn. In the given molecule the parent carbon skeleton is 3 membered linear chain and the root name for this molecule should be termed as propane.
The carbon chain should be numbered such that the substituent present in the molecule should given the least number in the carbon chain.
The substituents Br and CH3 present in the molecule should be termed as bromo and methyl respectively according to their alphabetical order which is the prefix part should be written along with the number to which position it is attached.
Therefore the systematic name is 2-bromo-2-methylpropane.
Find the common name for the given molecule. By considering the number of carbon atoms attached.
It contains
Therefore the common name for the given molecule is tert-butylbromide.
Conclusion
The systematic name and the common name for the given molecules are identified by using the atoms attached to the respective carbon with the help of using IUPAC nomenclature rules and R,S- configurations.
(c)
Interpretation:
The systematic name and common name for the given set of molecules should be identified.
Concept introduction:
Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…
Suffix represents the substituent present in the molecule. It can be any alkene, alkyne, alcohol, carboxylic acid, alcohol etc...
Root word represents the longest continuous carbon skeleton present in the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.
Common Name: It is quiet opposite to systematic name which is used for branched groups.
Chirality: It refers to a Carbon atom in a molecule that contains four different substituents.
Enantiomers: they are chiral molecules whose mirror images are not superimposable.
R and S nomenclature: it is used to assign the molecule using CIP rules.
The CIP rules are as follows:
Select the chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it.
If the numbering follows clockwise direction then the molecule is termed as R and if it follows anti-clockwise direction then molecule is termed as S.
(c)
Answer to Problem 47PP
Systematic name: 1-iodopropane and the common name: propyl iodide.
Explanation of Solution
Find the longest carbon chain in the given molecule and number it accordingly so that the substituent in the molecule present in the least numbered carbon atoms.
The given molecule is drawn. In the given molecule the parent carbon skeleton is 3 membered linear chain and the root name for this molecule should be termed as propane.
The carbon chain should be numbered such that the substituent present in the molecule should be given the least number in the carbon chain.
The substituent I present in the molecule should be termed as iodo which is the prefix part should be written along with the number to which it is attached.
Therefore the systematic name for the given molecule is 1-iodopropane.
Find the common name for the given molecule.
It is termed as propyl since it contains –CH2CH2CH3 and also it contains one iodine group which should be suffixed using ide.
Therefore the common name for the given molecule is propyl-iodide.
Conclusion
The systematic name and the common name for the given molecules are identified by using the atoms attached to the respective carbon with the help of using IUPAC nomenclature rules and R,S- configurations.
(d)
Interpretation:
The systematic name and common name for the given set of molecules should be identified.
Concept introduction:
Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…
Suffix represents the substituent present in the molecule. It can be any alkene, alkyne, alcohol, carboxylic acid, alcohol etc...
Root word represents the longest continuous carbon skeleton present in the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.
Common Name: It is quiet opposite to systematic name which is used for branched groups.
Chirality: It refers to a Carbon atom in a molecule that contains four different substituents.
Enantiomers: they are chiral molecules whose mirror images are not superimposable.
R and S nomenclature: it is used to assign the molecule using CIP rules.
The CIP rules are as follows:
Select the chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it.
If the numbering follows clockwise direction then the molecule is termed as R and if it follows anti-clockwise direction then molecule is termed as S.
(d)
Answer to Problem 47PP
Systematic name: (R)-2-bromobutane and the common name: (R)-sec-butyl bromide.
Explanation of Solution
Find the longest carbon chain in the given molecule and number it accordingly so that the substituent in the molecule present in the least numbered carbon atoms.
The given molecule is drawn. In the given molecule the parent carbon skeleton is 4 membered linear chain and the root name for this molecule should be termed as butane.
The substituent
This molecule contains chiral carbon so the atoms around the carbon atoms are numbered and the numbering results in clockwise direction termed as R which is to be placed in first part of the name.
Therefore the systematic name for the given molecule is (R)-2-bromobutane.
Find the common name for the given molecule.
It is termed as sec-butyl since it contains
This molecule contains one chiral carbon so the atoms around the carbon atoms are numbered and the numbering results in clockwise direction termed as R which is to be placed in first part of the name.
Therefore the common name for the given molecule is (R)-sec-butylbromide.
Conclusion
The systematic name and the common name for the given molecules are identified by using the atoms attached to the respective carbon with the help of using IUPAC nomenclature rules and R,S- configurations.
(e)
Interpretation:
The systematic name and common name for the given set of molecules should be identified.
Concept introduction:
Systematic Name: It is a standardized name given for a chemical compound in systematic manner. Any organic molecule can be named by using IUPAC (International Union for Pure and applied chemistry) rules. IUPAC name consists of three parts in major namely Prefix suffix and root word.
Prefix represents the substituent present in the molecule. It can be any alkyl group and carboxy, amino, cyano etc…
Suffix represents the substituent present in the molecule. It can be any alkene, alkyne, alcohol, carboxylic acid, alcohol etc...
Root word represents the longest continuous carbon skeleton present in the organic molecule.
When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo.
Common Name: It is quiet opposite to systematic name which is used for branched groups.
Chirality: It refers to a Carbon atom in a molecule that contains four different substituents.
Enantiomers: they are chiral molecules whose mirror images are not superimposable.
R and S nomenclature: it is used to assign the molecule using CIP rules.
The CIP rules are as follows:
Select the chiral carbon and assign the numbers according to the decreasing atomic mass of atoms attached to it.
If the numbering follows clockwise direction then the molecule is termed as R and if it follows anti-clockwise direction then molecule is termed as S.
(e)
Answer to Problem 47PP
Systematic name: 1-choloro-2, 2-dimethylpropane and the common name: neo-pentylchloride.
Explanation of Solution
Find the longest carbon chain in the given molecule and number it accordingly so that the substituent in the molecule present in the least numbered carbon atoms.
The given molecule is drawn.
In the given molecule the parent carbon skeleton is 3 membered linear chain and the root name for this molecule should be termed as propane.
The substituents Cl and two methyl groups present in the molecule should be termed as chloro and dimethyl respectively according to their alphabetical order which serves as the prefix part should be written along with the number to where it is attached.
Therefore the systematic name for the given molecule is 1-choloro-2,2dimethylpropane.
Find the common name for the given molecule.
It is termed as neo-pentyl since it is doubly branched and contains five carbon atoms. The substituent
Therefore the common name for the given molecule is neo-pentylchloride.
Conclusion
The systematic name and the common name for the given molecules are identified by using the atoms attached to the respective carbon with the help of using IUPAC nomenclature rules and R,S- configurations.
Want to see more full solutions like this?
Chapter 7 Solutions
Organic Chemistry
- Which of the following orbitals intersect or overlap the x-axis in the standard cartesian coordinate system used? (Select ALL correct answers.) Group of answer choices px dxz dx2-y2 py dxy sarrow_forwardWhich of the following sets of elements is not a Dobereiner triad? (Choose the best answer.) Group of answer choices Li-Na-K Al-Ga-In Cr-Mo-W K-Rb-Csarrow_forwardDon't used Ai solution and don't used hand raitingarrow_forward
- Don't used hand raiting and don't used Ai solutionarrow_forwardGive the structure(s) of the product(s) the reaction below, and be sure to indicate any relative stereochemistry (you can assume that each of the Diels-Alder reactions will proceed with endo selectivity). Draw out relevant enantiomer(s) if they are expected to form. If no reaction is expected to occur under the indicated conditions, then write "no reaction" or NR, and explain why you would expect nothing to occur. If more than one product is formed, please indicate which one will be the major product or if they will be formed in equal amounts. In all cases, equimolar amounts of both components/reagents are present unless indicated otherwise I'm struggling to see how this reaction will go! I am wondering if it will cycle on itself but I'm not sure how I drew out a decagon but I'm a bit lostarrow_forwardGive the structure(s) of the product(s) for the reactions below, and be sure to indicate any relative stereochemistry (you can assume that each of the Diels-Alder reactions will proceed with endo selectivity). Draw out relevant enantiomer(s) if they are expected to form. If no reaction is expected to occur under the indicated conditions, then write "no reaction" or NR, and explain why you would expect nothing to occur. If more than one product is formed, please indicate which one will be the major product or if they will be formed in equal amounts. In all cases, equimolar amounts of both components/reagents are present unless indicated otherwise .arrow_forward
- Calculate the residence time of strontium (Sr2+) in the world ocean, given that the average concentration of strontium in the world’s rivers is approximately 0.87 µmol L-1 (5 pts).arrow_forwardA package contains 1.33lbs of ground round. If it contains 29% fat, how many grams of fat are in the ground? arrow_forwardHow is the resonance structure formed to make the following reaction product. Please hand draw the arrows showing how the electrons move to the correct position. Do not use an AI answer. Please draw it yourself or don't bother.arrow_forward
- Part II Calculate λ max of the following compounds using wood ward- Fiecer rules a) b) c) d) e) OH OH dissolved in dioxane Br Br dissolved in methanol. NH₂ OCH 3 OHarrow_forward6. Match each of the lettered items in the column on the left with the most appropriate numbered item(s) in the column on the right. Some of the numbered items may be used more than once and some not at all. a. Z = 37 1. b. Mn 2. C. Pr element in period 5 and group 14 element in period 5 and group 15 d. S e. [Rn] 7s¹ f. d block metal 3. highest metallic character of all the elements 4. paramagnetic with 5 unpaired electrons 5. 4f36s2 6. isoelectronic with Ca²+ cation 7. an alkaline metal 8. an f-block elementarrow_forwardDraw all formal charges on the structures below as is and draw 1 resonance structure that is more stable.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