Concept explainers
(a)
Interpretation:
The type of organic compound which is nepetalactone needs to be determined.
Concept introduction:
The type of an organic compound depends on the arrangement of different elements present in it. It depends on the different
Explanation of Solution
Nepetalactone is known to be bicyclic monoterpenoid organic compound. There are 10 carbon atoms which are derived from isoprene having 2 fused rings. Out of the 2 rings, 1 is cyclopentane and other is lactone. The compound belongs to the class of iridoids.
(b)
Interpretation:
The structural formula for nepetalactone needs to be drawn with missing hydrogen atoms.
Concept introduction:
A structural formula tells about the actual number of atoms present in the molecule as well as their arrangement in the molecule.
Explanation of Solution
The given structure of nepetalactone is as follows:
Here, H atoms are missing in the structure thus the complete structure with H atoms is represented as follows:
(c)
Interpretation:
The molecular formula of the given nepetalactone needs to be determined.
Concept introduction:
The molecular formula tells about the actual number of atoms of different elements present in the molecule.
Explanation of Solution
The given structure of nepetalactone is as follows:
Here, H atoms are missing in the structure thus the complete structure with H atoms is represented as follows:
From the above structure, there are 10 carbon atoms, 14 hydrogen atoms and 2 oxygen atoms. Thus, the molecular formula is
Chapter 22 Solutions
Chemistry: Matter and Change
Additional Science Textbook Solutions
Brock Biology of Microorganisms (15th Edition)
Anatomy & Physiology (6th Edition)
Applications and Investigations in Earth Science (9th Edition)
Campbell Essential Biology (7th Edition)
Campbell Biology in Focus (2nd Edition)
Human Physiology: An Integrated Approach (8th Edition)
- Aktiv Learning App Cengage Digital Learning Part of Speech Table for Assign x o Mail-Karen Ento-Outlook * + app.aktiv.com Your Aktiv Learning trial expires on 02/06/25 at 01:15 PM Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. Problem 17 of 30 Drawing Arrows heat 4 O M B D 5x H H Und Settings H Done :0: H Jararrow_forwardConvert the following chairs into ring representations: a. Brz b.arrow_forwardDrawing Arrows 1 I I 1 heat 1 51 MO + Drag To Und Settings Done 0 0 Jan 31 3:5arrow_forward
- Don't used hand raitingarrow_forwardGramicidin A can adopt more than one structure; NMR spectroscopy has revealed an “end-to-end” dimer form, and x-ray crystallography has revealed an “anti-parallel double- helical” form. Briefly outline and describe an experimentalapproach/strategy to investigate WHICH configuration (“end-to-end dimer” vs “anti-paralleldouble helical”) gramicidin adopts in an actual lipid bilayer.arrow_forwardDon't used hand raitingarrow_forward
- CHEM2323 Problem 2-24 Tt O e: ל Predict the product(s) of the following acid/base reactions. Draw curved arrows to show the formation and breaking of bonds. If the bonds needed are not drawn out, you should redraw them. + BF3 (a) (b) HI + (c) OH -BF Problem 2-25 Use curved arrows and a proton (H+) to draw the protonated form of the following Lewis bases. Before starting, add all missing lone pairs. (a) (b) :0: (c) N 1 CHEM2323 PS CH02 Name:arrow_forwardCHEM2323 Problem 2-26 Tt O PS CH02 Name: Use the curved-arrow formalism to show how the electrons flow in the resonance form on the left to give the one on the right. (Draw all lone pairs first) (a) NH2 NH2 + (b) Problem 2-27 Double bonds can also act like Lewis bases, sharing their electrons with Lewis acids. Use curved arrows to show how each of the following double bonds will react with H-Cl and draw the resulting carbocation. (a) H2C=CH2 (b) (c) Problem 2-28 Identify the most electronegative element in each of the following molecules: (a) CH2FCI F Problem 2-29 (b) FCH2CH2CH2Br (c) HOCH2CH2NH2 (d) CH3OCH2Li F 0 0 Use the electronegativity table in Figure 2.3 to predict which bond in the following pairs is more polar and indicate the direction of bond polarity for each compound. (a) H3C-Cl or Cl-CI (b) H3C-H or H-CI (c) HO-CH3 or (CH3)3Si-CH3 (d) H3C-Li or Li-OHarrow_forwardDon't used hand raitingarrow_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