
(a)
Interpretation:
Molecular formula of hexanol must be given.
Concept introduction:
Molecular formula is the general formula of the molecule which shows the number of different atoms.

Answer to Problem 5E
Molecular formula of hexanol is C6H14O.
Explanation of Solution
Aliphatic alcohol has general formula CnH2n + 2O. As in hexanol there are 6 carbon atoms, so total number of hydrogen must be 14. There is one O atom which is present in the hydroxyl (alcoholic OH)
(b)
Interpretation:
A possible structural formula of hexanol must be drawn.
Concept introduction:
Structural formula is the representation of a molecule in which the arrangements of all the atoms are shown.

Answer to Problem 5E
Structural formula of hexanol is shown below.
Explanation of Solution
One possible structural formula of hexanol acid is drawn in which all the carbon atoms have 4 bonds. The O has two bonds and two lone pairs of electrons. There is no lone pair on C and H atoms. Hydrogen atoms of the carbon chain are not shown to avoid complexity of the structure.
Many hexanol possibly depend on the position of functional (alcoholic OH) group.
(c)
Interpretation:
Whether molecular formula or structural formula is more important in determining the smell of the compound must be explained.
Concept introduction:
Structural formula gives more information regarding three dimensional arrangements of atoms and shape of a molecule whereas molecular formula only gives number of different atoms.

Answer to Problem 5E
Structural formula is more important in determining the smell of a compound.
Explanation of Solution
The functional group (OH) present in hexanol is shown in red. The functional group is present in carbon-1. The structure of the hexanol will change if the OH group is present in other carbons. Thus, to get the actual shape of the molecule, structural formula is essential. Many structures can be drawn for a single molecular formula. So, to determine the smell of a compound, the idea of shape of the molecule is important. Thus, structural formula is more important than molecular formula in determining the smell of a molecule.
Chapter U2 Solutions
Living by Chemistry
Additional Science Textbook Solutions
Campbell Biology: Concepts & Connections (9th Edition)
Campbell Biology (11th Edition)
Physics for Scientists and Engineers: A Strategic Approach, Vol. 1 (Chs 1-21) (4th Edition)
Microbiology: An Introduction
Microbiology: An Introduction
Campbell Biology in Focus (2nd Edition)
- Identify as E1 or E2 and write the mechanism.arrow_forwardIdentify if their reaction is most likely SN1 or SN2 mechanism.arrow_forwardDraw the products formed when the following alkene is treated with 03 followed by Zn, H₂O. Be sure to answer all parts. draw structure ... smaller molar mass product draw structure ... larger molar mass productarrow_forward
- Identify as SN1 or SN2 and write the mechanism.arrow_forwardComplete the reaction. Not the mechanism.arrow_forwardDraw the mechanism using the arrows on conventions, including all formal charges and correct arrows. If stereochemical distinction can be made they should be included in the structure of the products.arrow_forward
- Draw the epoxide formed when the following alkene is treated with mCPBA. Click the "draw structure" button to launch the drawing utility. draw structure ...arrow_forwardRank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. Explanation Check CF3 (Choose one) OH (Choose one) H (Choose one) (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacyarrow_forwardIdentifying electron-donating and electron-withdrawing effects For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects Resonance Effects Overall Electron-Density CF3 O donating O donating O electron-rich O withdrawing withdrawing O no inductive effects O no resonance effects O electron-deficient O similar to benzene OCH3 Explanation Check O donating O donating ○ withdrawing withdrawing O no inductive effects no resonance effects electron-rich electron-deficient O similar to benzene Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_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





