Concept explainers
(a)
Interpretation:
The IUPAC name of the cyclopentyl iodide is to be written.
Concept introduction:
Select the longest continuous chain or largest carbon ring as a parent chain. The name of the corresponding
(b)
Interpretation:
The IUPAC name of the n-hexyl bromide is to be written.
Concept introduction:
Select the longest continuous chain or largest carbon ring as a parent chain. The name of the corresponding alkane will be the root of the molecule’s name. Find out the substituent and add the name of the substituent as a prefix to the left of the root. The locator number is given to the carbon atom. The locator number is written to the left of the substituent name and a hyphen is added to separate the locator number from the remaining name.
Want to see the full answer?
Check out a sample textbook solutionChapter A Solutions
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
- Please answer with explanationsarrow_forwardPlease see image for question.arrow_forwardProblem: (a) Draw six (6) constitutional isomers of C6H1202. (b) Which of the compounds you drew would be the most soluble in water? Explain your choice. (c) Which of the compounds you drew would be the most soluble in hexane? Explain your choice.arrow_forward
- Solve correctly please, need all subparts with some explanation also.arrow_forwardQuestion 1 What is the correct IUPAC name of the following compound? Problem viewing the image. Click Preview Here O 2-methylpent-2-en-2-one O 4-methyl-3-pentenal O 2-methylpent-2-en-4-one O 4-methylpent-3-en-2-onearrow_forwardWhat is the IUPAC name of the compound shown here? (view attatchement) **FIRST TIME YOU ANSWERE THIS WAS WRONG, please help with correct answer. The answer you gave me before was 1,4-dimethylcyclobut-1-ene but is was WRONG . This is what the paragraph also said next to the question "Alkanes are called saturated hydrocarbons because each carbon atom has the maximum number of hydrogen atoms. In contrast, alkenes and alkynes are unsaturated because they contain double or triple bonds that reduce the number of hydrogen atoms in the compound. When naming unsaturated hydrocarbons, a suffix reflects the type of multiple bond in the compound: ene is used for alkenes (double bond), and yne is used for alkynes (triple bond). For cyclic alkenes and alkynes, the ring is numbered such that the double or triple bond is between the first two carbon atoms. For straight-chain molecules, the numbering starts at one end of the chain, so the location of the double or triple bond must be…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