Pearson eText Organic Chemistry -- Instant Access (Pearson+)
8th Edition
ISBN: 9780135213711
Author: Paula Bruice
Publisher: PEARSON+
expand_more
expand_more
format_list_bulleted
Question
Chapter 5, Problem 53P
(a)
Interpretation Introduction
Interpretation:
Possible geometric isomers for the given compound should be drawn and these isomers have to be named.
Concept introduction:
- Molecular structure is the arrangement of
chemical bonds between atoms in a molecule (or in an ion or radical with multiple atoms), specifically which atoms are chemically bonded to what other atoms with what kind of chemical bond. From the IUPAC name of compound its structure can be easily drawn. - IUPAC name consists of three parts in major namely Prefix suffix and root word.
- Prefix represents the substituent present in the molecule and its position in the root name.
- Suffix denotes the presence of
functional group if any in the molecule. It can be an alkene,alkyne , alcohol,carboxylic acid , alcohol etc. - For
alkenes , suffix will be ‘ene’. - Root word represents the longest continuous carbon skeleton of the organic molecule.
- When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo, if it is two cyclic structure combined then prefixed with bicyclo.
- E-Z designators are used as like cis-trans terminology for non-similar groups attached alkenes.
- In E-Z designations, the groups attached to vinylic positions are checked by their priority on the basis of higher molecular weight.
- If the higher priority groups are on the same sides, then the configuration is designated as Z. If the higher priority groups are on the opposite sides, then the configuration is designated as E.
(b)
Interpretation Introduction
Interpretation:
Possible geometric isomers for the given compound should be drawn and these isomers have to be named.
Concept introduction:
- Molecular structure is the arrangement of chemical bonds between atoms in a molecule (or in an ion or radical with multiple atoms), specifically which atoms are chemically bonded to what other atoms with what kind of chemical bond. From the IUPAC name of compound its structure can be easily drawn.
- IUPAC name consists of three parts in major namely Prefix suffix and root word.
- Prefix represents the substituent present in the molecule and its position in the root name.
- Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
- For alkenes, suffix will be ‘ene’.
- Root word represents the longest continuous carbon skeleton of the organic molecule.
- When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo, if it is two cyclic structure combined then prefixed with bicyclo.
- E-Z designators are used as like cis-trans terminology for non-similar groups attached alkenes.
- In E-Z designations, the groups attached to vinylic positions are checked by their priority on the basis of higher molecular weight. If the higher priority groups are on the same sides, then the configuration is designated as Z. If the higher priority groups are on the opposite sides, then the configuration is designated as E.
(c)
Interpretation Introduction
Interpretation:
Possible geometric isomers for the given compound should be drawn and these isomers have to be named.
Concept introduction:
- Molecular structure is the arrangement of chemical bonds between atoms in a molecule (or in an ion or radical with multiple atoms), specifically which atoms are chemically bonded to what other atoms with what kind of chemical bond. From the IUPAC name of compound its structure can be easily drawn.
- IUPAC name consists of three parts in major namely Prefix suffix and root word.
- Prefix represents the substituent present in the molecule and its position in the root name.
- Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
- For alkenes, suffix will be ‘ene’.
- Root word represents the longest continuous carbon skeleton of the organic molecule.
- When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo, if it is two cyclic structure combined then prefixed with bicyclo.
- E-Z designators are used as like cis-trans terminology for non-similar groups attached alkenes.
- In E-Z designations, the groups attached to vinylic positions are checked by their priority on the basis of higher molecular weight. If the higher priority groups are on the same sides, then the configuration is designated as Z. If the higher priority groups are on the opposite sides, then the configuration is designated as E.
(d)
Interpretation Introduction
Interpretation:
Possible geometric isomers for the given compound should be drawn and these isomers have to be named.
Concept introduction:
- Molecular structure is the arrangement of chemical bonds between atoms in a molecule (or in an ion or radical with multiple atoms), specifically which atoms are chemically bonded to what other atoms with what kind of chemical bond. From the IUPAC name of compound its structure can be easily drawn.
- IUPAC name consists of three parts in major namely Prefix suffix and root word.
- Prefix represents the substituent present in the molecule and its position in the root name.
- Suffix denotes the presence of functional group if any in the molecule. It can be an alkene, alkyne, alcohol, carboxylic acid, alcohol etc.
- For alkenes, suffix will be ‘ene’.
- Root word represents the longest continuous carbon skeleton of the organic molecule.
- When a molecule consists of cyclic structure, the root word of the molecule is prefixed with cyclo, if it is two cyclic structure combined then prefixed with bicyclo.
- E-Z designators are used as like cis-trans terminology for non-similar groups attached alkenes.
- In E-Z designations, the groups attached to vinylic positions are checked by their priority on the basis of higher molecular weight. If the higher priority groups are on the same sides, then the configuration is designated as Z. If the higher priority groups are on the opposite sides, then the configuration is designated as E.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
What is the lone pair or charge that surrounds the nitrogen here to give it that negative charge?
Last Name, Firs
Statifically more chances to abstract one of these 6H
11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4
• 6H total $ 4th total
21 total
4H total
ZH
2H
Statistical
H < 3°C-H werkst
-
product
bund abstraction here
leads to the mo favored
a) (6pts) How many unique mono-chlorinated products can be formed and what are the
structures for the thermodynamically and statistically favored products?
Proclict
6
Number of Unique
Mono-Chlorinated Products
f
Thermodynamically
Favored Product
Statistically
Favored Product
b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the
formation of the thermodynamically favored product. Only draw the p-1 step. You do
not need to include lone pairs of electrons. No enthalpy calculation necessary
'H
H-Cl
Waterfox
2. (a) Many main group oxides form acidic solutions when added to water. For example solid
tetraphosphorous decaoxide reacts with water to produce phosphoric acid. Write a balanced
chemical equation for this reaction.
(b) Calcium phosphate reacts with silicon dioxide and carbon graphite at elevated temperatures
to produce white phosphorous (P4) as a gas along with calcium silicate (Silcate ion is SiO3²-)
and carbon monoxide. Write a balanced chemical equation for this reaction.
Chapter 5 Solutions
Pearson eText Organic Chemistry -- Instant Access (Pearson+)
Ch. 5.1 - What is the molecular formula for each of the...Ch. 5.1 - Prob. 4PCh. 5.1 - Determine the degree of unsaturation and then draw...Ch. 5.1 - Prob. 6PCh. 5.2 - What is each compounds systematic name?Ch. 5.2 - Prob. 8PCh. 5.2 - Draw the structure for each of the following: a....Ch. 5.3 - How many carbons are in the planar double-bond...Ch. 5.3 - Prob. 12PCh. 5.5 - Prob. 13P
Ch. 5.5 - Prob. 14PCh. 5.5 - Prob. 16PCh. 5.5 - Prob. 17PCh. 5.6 - a. Which of the monosubstituted cyclohexanes in...Ch. 5.6 - a. Calculate the percentage of isopropylcylohexane...Ch. 5.6 - a. for which reaction in each set will S be more...Ch. 5.6 - a. For a reaction with H = 12 kcal/ mol and S =...Ch. 5.8 - Prob. 23PCh. 5.9 - Prob. 24PCh. 5.9 - How many different alkenes can be hydrogenated to...Ch. 5.9 - The same alkane is obtained from the catalytic...Ch. 5.9 - Prob. 27PCh. 5.9 - Rank the following compounds from most stable to...Ch. 5.10 - Prob. 29PCh. 5.10 - Prob. 30PCh. 5.11 - The rate constant for a reaction can be increased...Ch. 5.11 - Prob. 33PCh. 5.11 - a. Which reaction has a greater equilibrium...Ch. 5.12 - Draw a reaction coordinate diagram for a two-step...Ch. 5.12 - a. Which step in the reaction coordinate diagram...Ch. 5.12 - Draw a reaction coordinate diagram for the...Ch. 5.13 - Prob. 38PCh. 5 - What is each compounds systematic name?Ch. 5 - Prob. 40PCh. 5 - Draw the structure of a hydrocarbon that has six...Ch. 5 - Draw the condensed structure for each of the...Ch. 5 - Prob. 43PCh. 5 - Prob. 44PCh. 5 - Prob. 45PCh. 5 - Name the following:Ch. 5 - Prob. 47PCh. 5 - Prob. 48PCh. 5 - Prob. 49PCh. 5 - In a reaction in which reactant A is in...Ch. 5 - Which bond is stronger? Briefly explain why.Ch. 5 - Prob. 52PCh. 5 - Prob. 53PCh. 5 - By following the curved red arrows, draw the...Ch. 5 - Prob. 55PCh. 5 - Prob. 56PCh. 5 - Draw structures for the following: a....Ch. 5 - Prob. 58PCh. 5 - a. Which of the following reactions has the larger...Ch. 5 - Prob. 60PCh. 5 - a. What is the equilibrium constant for a reaction...Ch. 5 - Prob. 62PCh. 5 - Prob. 63PCh. 5 - Given that the free energy of the twist-boat...Ch. 5 - Prob. 65PCh. 5 - Prob. 1PCh. 5 - Prob. 2PCh. 5 - Prob. 3PCh. 5 - Prob. 4PCh. 5 - Prob. 5PCh. 5 - Prob. 6PCh. 5 - Draw curved arrows to show the movement of the...Ch. 5 - Prob. 8PCh. 5 - Prob. 9PCh. 5 - Prob. 10P
Knowledge Booster
Similar questions
- this is an organic chemistry question please answer accordindly!! please post the solution in your hand writing not an AI generated answer please draw the figures and structures if needed to support your explanation hand drawn only!!!! answer the question in a very simple and straight forward manner thanks!!!!! im reposting this please solve all parts and draw it not just word explanations!!arrow_forward2B: The retrosynthetic cut below provides two options for a Suzuki coupling, provide the identities of A, B, C and D then identify which pairing is better and justify your choice. O₂N. Retro-Suzuki NO2 MeO OMe A + B OR C + Darrow_forwardthis is an organic chemistry question please answer accordindly!! please post the solution in your hand writing not an AI generated answer please draw the figures and structures if needed to support your explanation hand drawn only!!!! answer the question in a very simple and straight forward manner thanks!!!!! im reposting this please solve all parts and draw it not just word explanations!!arrow_forward
- A buffered solution containing dissolved aniline, CH,NH2, and aniline hydrochloride, CH, NH, Cl, has a pH of 5.41. Determine the concentration of CH, NH in the solution if the concentration of CH, NH, is 0.305 M. The pK of aniline is 9.13. [CHẠNH] = Calculate the change in pH of the solution, ApH, if 0.375 g NaOH is added to the buffer for a final volume of 1.40 L. Assume that any contribution of NaOH to the volume is negligible. ApH = Marrow_forwardShow work. don't give Ai generated solutionarrow_forwardShow work. don't give Ai generated solutionarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- 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
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY