(a)
Interpretation:
The structure should be drawn for each of the given (IUPAC) molecule.
Concept introduction:
Systematic Name :It is 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 names consist of three parts in major namely prefix and word.
Prefix represents the substituent present in the molecule .it can be any alkyl group and
Suffix represent the substituent present in the
molecule. It can be any
Root word represents the longest continuous carbon skeleton present in the organic molecule.
Common Name it is quite opposite to systematic name which is used for branched groups.
Chirality It refers to a carbon atom in a molecule that contain four different substituents.
Enantiomers: they are chiral molecule whose mirror images are not superimposable.
R&S Nomenclature: It is used to assign the molecule using the CIP rules.
The CIP-rules are as follows:
Select the chiral carbon and assign the number according to the decreasing
If the numbering follows clockwise direction then molecule is term R and if it follows anti-clockwise direction then molecule is termed as S.
(b)
Interpretation:
The structure should be drawn for each of the given (IUPAC) molecule.
Concept introduction:
Systematic Name :It is 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 names consist of three parts in major namely prefix and word.
Prefix represents the substituent present in the molecule .it can be any alkyl group and carboxylic acid, alcohol etc.…
Suffix represent 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.
Common Name it is quite opposite to systematic name which is used for branched groups.
Chirality It refers to a carbon atom in a molecule that contain four different substituents.
Enantiomers: they are chiral molecule whose mirror images are not superimposable.
R&S Nomenclature: It is used to assign the molecule using the CIP rules.
The CIP-rules are as follows:
Select the chiral carbon and assign the number according to the decreasing atomic mass of atom attached to it.
If the numbering follows clockwise direction then molecule is term R and if it follows anti-clockwise direction then molecule is termed as S.
(c)
Interpretation:
The structure should be drawn for each of the given (IUPAC) molecule.
Concept introduction:
Systematic Name :It is 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 names consist of three parts in major namely prefix and word.
Prefix represents the substituent present in the molecule .it can be any alkyl group and carboxylic acid, alcohol etc.…
Suffix represent 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.
Common Name it is quite opposite to systematic name which is used for branched groups.
Chirality It refers to a carbon atom in a molecule that contain four different substituents.
Enantiomers: they are chiral molecule whose mirror images are not superimposable.
R&S Nomenclature: It is used to assign the molecule using the CIP rules.
The CIP-rules are as follows:
Select the chiral carbon and assign the number according to the decreasing atomic mass of atom attached to it.
If the numbering follows clockwise direction then molecule is term R and if it follows anti-clockwise direction then molecule is termed as S.
Want to see the full answer?
Check out a sample textbook solutionChapter 20 Solutions
Organic Chemistry
- 2. A graph shown below shows first ionization energies for elements from H to Ne. First ionization energy/kJ mol 2500 2000 1500 1000 500 T T T T 1 2 3 5 6 7 8 9 10 Atomic number a) Using arguments of electronic structure, explain why ionization energy of Li is much lower than that of H. (2 points) then dips at O. b) Using the same arguments, explain why ionization energy increases from B to N, and (3 points)arrow_forwardGive the name of this compound, including stereochemistry if relevant: CICH2 CH3 Br CH₂CH=CH2 Write in the product, including stereochemistry where relevant, for these reactions. See end of ch. 8, p. 301-303. 1. 03 a) 2-methyl-2-pentene -> 2. Zn, H* Br2 b) 1-ethylcyclopentene -->arrow_forwardNonearrow_forward
- 3. You may want to read paragraph 1.5 in your textbook before answering this question. Give electron configuration (short-hand notation is fine) for: (5 points) 3+ a) Manganese atom and Mn³+ b) Se atom c) Cu atom and Cu+arrow_forwardPlease correct answer and don't use hand ratingarrow_forwardNonearrow_forward
- Nonearrow_forwardHowever, why are intermolecular forces in metallic and ionic compounds not discussed as extensively? Additionally, what specific types of intermolecular attractions exist in metals and ionic compoundsarrow_forwardWhat is the preparation of 1 Liter of 0.1M NH4Cl buffer at pH 9.0 with solid NH4Cl and 0.1M NaOH. How would I calculate the math to describe this preparation? How would I use Henderson-Hasselbach equation?arrow_forward
- C Predict the major products of this organic reaction. Be sure you use wedge and dash bonds when necessary, for example to distinguish between major products with different stereochemistry. : ☐ + x G C RCO₂H Click and drag to start drawing a structure.arrow_forwardFill in the blanks by selecting the appropriate term from below: For a process that is non-spontaneous and that favors products at equilibrium, we know that a) ΔrG∘ΔrG∘ _________, b) ΔunivSΔunivS _________, c) ΔsysSΔsysS _________, and d) ΔrH∘ΔrH∘ _________.arrow_forwardHighest occupied molecular orbital Lowest unoccupied molecular orbital Label all nodes and regions of highest and lowest electron density for both orbitals.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