Concept explainers
Interpretation:
The name of the following compound should be determined:
Concept introduction:
When the carbon atoms of hydrocarbons are arranged in such a way that it results in the formation of ring then it is said to be cycloalkanes.

Answer to Problem 58A
1, 2, 4-trimethylcyclohexane.
Explanation of Solution
In order to give the name to the cycloalkane following steps are followed:
1. The parent (longest) continuous carbon chain is identified.
2. The prefix -cyclo is used before the name of
3. If the attached alkyl chain possesses greater number of carbon atoms, then alkyl chain is considered as primary parent chain.
4. Name should be written in alphabetical order and numbering should be done in such a way that the substituent group gets lowest number.
5. Hyphen is used to connect the number to the name.
The given structure is:
The parent chain contains a ring of six carbon atoms and 3 substituents so numbering is done in such a way that substituent gets lower number as shown:
Since, the parent chain contains a ring of six carbon atoms and only single bonds are present so, the parent chain is cyclohexane. Since, the substituent,
Interpretation:
The name of the following compound should be determined:
Concept introduction:
When the carbon atoms of hydrocarbons are arranged in such a way that it results in the formation of ring then it is said to be cycloalkanes.

Answer to Problem 58A
1-ethyl-3-methylcyclopentane.
Explanation of Solution
The given structure is:
The parent chain contains a ring of five carbon atoms and 2 substituents so numbering is done in such a way that substituent gets lower number as shown:
Since, the parent chain contains a ring of five carbon atoms and only single bonds are present so, the parent chain is cyclopentane. Since, the substituent,
Interpretation:
The name of the following compound should be determined:
Concept introduction:
When the carbon atoms of hydrocarbons are arranged in such a way that it results in the formation of ring then it is said to be cycloalkanes.

Answer to Problem 58A
1-methyl-3-propylcyclobutane.
Explanation of Solution
The given structure is:
The parent chain contains a ring of four carbon atoms and 2 substituents so numbering is done in such a way that substituent gets lower number as shown:
Since, the parent chain contains a ring of four carbon atoms and only single bonds are present so, the parent chain is cyclobutane. Since, the substituent,
Interpretation:
The name of the following compound should be determined:
Concept introduction:
When the carbon atoms of hydrocarbons are arranged in such a way that it results in the formation of ring then it is said to be cycloalkanes.

Answer to Problem 58A
6-ethyl-1, 2, 3-trimethylcyclooctane.
Explanation of Solution
The given structure is:
The parent chain contains a ring of eight carbon atoms and 4 substituents so numbering is done in such a way that substituent gets lower number as shown:
Since, the parent chain contains a ring of eight carbon atoms and only single bonds are present so, the parent chain is cyclooctane. Since, the substituent, 3
Chapter 21 Solutions
Chemistry: Matter and Change
Additional Science Textbook Solutions
Applications and Investigations in Earth Science (9th Edition)
Chemistry: The Central Science (14th Edition)
Genetic Analysis: An Integrated Approach (3rd Edition)
Anatomy & Physiology (6th Edition)
Organic Chemistry (8th Edition)
Chemistry: An Introduction to General, Organic, and Biological Chemistry (13th Edition)
- Provide an IUPAC name for each of the compounds shown. (Specify (E)/(Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) H₁₂C C(CH3)3 C=C H3C CH3 CH3CH2CH CI CH3 Submit Answer Retry Entire Group 2 more group attempts remaining Previous Nextarrow_forwardArrange the following compounds / ions in increasing nucleophilicity (least to most nucleophilic) CH3NH2 CH3C=C: CH3COO 1 2 3 5 Multiple Choice 1 point 1, 2, 3 2, 1, 3 3, 1, 2 2, 3, 1 The other answers are not correct 0000arrow_forwardcurved arrows are used to illustrate the flow of electrons. using the provided starting and product structures, draw the cured electron-pushing arrows for thw following reaction or mechanistic steps. be sure to account for all bond-breaking and bond making stepsarrow_forward
- Using the graphs could you help me explain the answers. I assumed that both graphs are proportional to the inverse of time, I think. Could you please help me.arrow_forwardSynthesis of Dibenzalacetone [References] Draw structures for the carbonyl electrophile and enolate nucleophile that react to give the enone below. Question 1 1 pt Question 2 1 pt Question 3 1 pt H Question 4 1 pt Question 5 1 pt Question 6 1 pt Question 7 1pt Question 8 1 pt Progress: 7/8 items Que Feb 24 at You do not have to consider stereochemistry. . Draw the enolate ion in its carbanion form. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. ⚫ Separate multiple reactants using the + sign from the drop-down menu. ? 4arrow_forwardShown below is the mechanism presented for the formation of biasplatin in reference 1 from the Background and Experiment document. The amounts used of each reactant are shown. Either draw or describe a better alternative to this mechanism. (Note that the first step represents two steps combined and the proton loss is not even shown; fixing these is not the desired improvement.) (Hints: The first step is correct, the second step is not; and the amount of the anhydride is in large excess to serve a purpose.)arrow_forward
- Hi I need help on the question provided in the image.arrow_forwardDraw a reasonable mechanism for the following reaction:arrow_forwardDraw the mechanism for the following reaction: CH3 CH3 Et-OH Et Edit the reaction by drawing all steps in the appropriate boxes and connecting them with reaction arrows. Add charges where needed. Electron-flow arrows should start on the electron(s) of an atom or a bond and should end on an atom, bond, or location where a new bond should be created. H± EXP. L CONT. י Α [1] осн CH3 а CH3 :Ö Et H 0 N о S 0 Br Et-ÖH | P LL Farrow_forward
- 20.00 mL of 0.150 M NaOH is titrated with 37.75 mL of HCl. What is the molarity of the HCl?arrow_forward20.00 mL of 0.025 M HCl is titrated with 0.035 M KOH. What volume of KOH is needed?arrow_forward20.00 mL of 0.150 M NaOH is titrated with 37.75 mL of HCl. What is the molarity of the HCl?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





