Concept explainers
How does the structure of a cycloalkane differ from that of a straight-chain or branched-chain

Interpretation:
The difference in structure of cycloalkane from that of a straight chain or branched-chain alkane needs to be explained.
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 53A
The difference in structure of cycloalkane from that of a straight chain or branched-chain alkane is that cycloalkanes contains 2 H atoms less than that of straight chain or branched-chain alkane.
Explanation of Solution
The general formula of alkane is
The branched chain of 5 carbon atoms will be:
For a cycloalkane formed from 5 carbon atoms, the structure and the molecular formula will be:
Cyclopentane that means it contains 5 carbon atoms and 10 hydrogen atoms.
Since, in cycloalkane the number of hydrogen atoms are less from alkane by 2 units so, the general formula of cycloalkane will be:
Hence, the difference in structure of cycloalkane from that of a straight chain or branched-chain alkane is that cycloalkanes contains 2 H atoms less than that of straight chain or branched-chain alkane.
Chapter 21 Solutions
Chemistry: Matter and Change
Additional Science Textbook Solutions
Genetic Analysis: An Integrated Approach (3rd Edition)
Human Anatomy & Physiology (2nd Edition)
Cosmic Perspective Fundamentals
Campbell Biology: Concepts & Connections (9th Edition)
Physics for Scientists and Engineers: A Strategic Approach, Vol. 1 (Chs 1-21) (4th Edition)
Organic Chemistry (8th Edition)
- 2. Identify the reagents you would need to achieve the following. You may need to consider using a protecting group. HO 1. 2. 3. 4. 5. OH Br HOarrow_forwardBeF2 exists as a linear molecule. Which kind of hybrid orbitals does Be use in this compound? Use Orbital Diagrams to show how the orbitals are formed. (6)arrow_forwardPlease answer the questions and provide detailed explanations as well as a drawing to show the signals in the molecule.arrow_forward
- Propose an efficient synthesis for the following transformation: EN The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A. t-BuOK B. Na2Cr2O7, H2SO4, H2O C. NBS, heat F. NaCN D. MeOH E. NaOH G. MeONa H. H2O I. 1) O3; 2) DMSarrow_forwardStereochemistry Identifying the enantiomer of a simple organic molecule 1/5 Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of t above box under the table. Br ま HO H 0 Molecule 1 Molecule 2 Molecule 3 OH H Br H H" Br OH Br Molecule 4 Br H OH + + OH Molecule 5 Br H OH none of the above Molecule 6 Br H... OHarrow_forwardPlease answer the questions and provide detailed explanations.arrow_forward
- Question 16 0/1 pts Choose the correct option for the following cycloaddition reaction. C CF3 CF3 CF3 CF3 The reaction is suprafacial/surafacial and forbidden The reaction is antarafacial/antarafacial and forbidden The reaction is antarafacial/antarafacial and allowed The reaction is suprafacial/surafacial and allowedarrow_forward1. Give the structures of the products obtained when the following are heated. Include stereochemistry where relevant. A NO2 + NO2 B + C N=C CEN + { 2. Which compounds would you heat together in order to synthesize the following?arrow_forwardExplain how myo-inositol is different from D-chiro-inositol. use scholarly sources and please hyperlink.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





