![Bundle: Introduction to General, Organic and Biochemistry, 11th + OWLv2, 4 terms (24 months) Printed Access Card](https://www.bartleby.com/isbn_cover_images/9781305705159/9781305705159_largeCoverImage.gif)
Concept explainers
(a)
Interpretation:
Using VSEPR Theory, the geometry of each central atom present in given structure of Androstenedione is to be identified.
Concept Introduction:
Bond angles in the molecules can be predicted by using valence shell electron pair repulsion (VSEPR) model. According to this model, the valence electrons of an atom are involved in the formation of single, double or triple bond. The valence electrons can also be unshared and exist as lone pair on atoms. The combination forms a negatively charged region of electron density around a nucleus. Since, like charges do not attract, the region of electron density around a nucleus spread out so that each atom is as far away from each other at different angles.
(b)
Interpretation:
Using VSEPR theory, the various relative bond angles associated with each central atom of the Androstenedione molecule is to be determined.
Concept Introduction:
Bond angles in the molecules can be predicted by using valence shell electron pair repulsion (VSEPR) model. According to this model, the valence electrons of an atom are involved in the formation of single, double or triple bond. The valence electrons can also be unshared and exist as lone pair on atoms. The combination forms a negatively charged region of electron density around a nucleus. Since, like charges do not attract, the region of electron density around a nucleus spread out so that each atom is as far away from each other at different angles.
1. Each carbon atom having all single bonds having tetrahedral geometry has bond angle
2. Each carbon atom having double bond having trigonal planner geometry has bond angle 120(.
(c)
Interpretation:
The most polar bond in androstenedione is to be predicted.
Concept Introduction:
A molecule is polar if it has polar bonds and the centers of its partial positive and partial negative charge do not coincide.
(d)
Interpretation:
Observing the bonds of Androstenedione molecule, it should be determined whether Androstenedione is polar or nonpolar.
Concept Introduction:
A molecule is polar if it has polar bonds and if the centers of partial positive charge and partial negative charge lie at different places with in the molecule.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 3 Solutions
Bundle: Introduction to General, Organic and Biochemistry, 11th + OWLv2, 4 terms (24 months) Printed Access Card
- Can you help me and explain the answers please.arrow_forwardB 1 of 2 Additional problems in preparation to Midterm #1: 1.) How can the following compounds be prepared using Diels-Alder reaction: CH3 O CN (a) (b) CN CH3 2.) What is the missing reagent in the shown reaction? H3C + ? H3C H3C CN H3C ''CN (၁) H 3.) Write the products 1,2-addition and 1,4-addition of DBr to 1,3-cyclohexadiene. Remember, D is deuterium, a heavy isotope of hydrogen. It reacts exactly like hydrogen. 4.) In the shown reaction, which will be the kinetic product and which will be the thermodynamic product? H3C CI H3C HCI H3C + 5.) Which of the following molecules is aromatic? (a) (b) (c) H 6.) Which of the following molecules is aromatic? (a) (b) (c) 7.) Write the mechanism for the shown reaction. + Ха AICI 3 CI 8.) Suggest reagents that would convert benzene into the shown compounds. CI NO2 -8-6-6-8-a (a) (b) (c) (d) (e) (a) SO3H Brarrow_forwardThe number of 2sp^2 hybridized atoms in is: A. 8; B. 6; C.4; D.2; E.0;arrow_forward
- The highest boiling compound from among the following isA. 2-methylheptane; B. 3-methylheptane; C. 2,2-dimethylhexane;D. octane; E. 2,2,3-trimethylpentanearrow_forwardWhich of the following features are found in the most stable structure ofCH5NO that does not have a CO bond?w. a π bond, x. two NH bonds, y. one OH bond, z. 3 lone pairsA. w, x; B. x, y; C. y, z; D. x, y, z; E. all of them.arrow_forwardWhich one of the following functional groups is not present in thecompound shownA. amine; B. aldehyde, C. ether; D. amide. E. ketonearrow_forward
- Which of the following formulas correspond to at least one compound inwhich resonance is important?w. C2H5N x. C3H5Br; y. C3H4; z. C4H6.A. w, x, y; B. x, y, z; C. w, x, z; D. w, y, z; E. all of themarrow_forwardPredict the product(s) that are formed after each step for reactions 1-4. In each case, consider formation of any chiral center(s) and draw all expected stereoisomers. 1) OH 1) HBr (SN2) 2) NaOH, heat 3) BH3, THF 4) H2O2, NaOH 2) OH 1) SOCI 2, py 2) NaOEt 3) Br2, H₂O 3) OH 1) H2SO4 conc. 2) HBr, ROOR 3) KOtBu 4) OH 1) TsCl, py 2) NaOEt 3) 03 4) DMSarrow_forwardWhich of the following rings has the least strain in its most stableconformation?A. Cyclobutane; B. Cyclopentane; C. Cyclohexane; D. Cycloheptane;E. Cyclooctanearrow_forward
- The number of different carbon skeletons that have a main chain of 9carbons and an ethyl branch isA 3; B. 4; C. 5; D. 6; E. 7arrow_forwardQ5: Classify the following pair of molecules as constitutional isomers, enantiomers, diastereomers, the same molecule, or completely different molecules. Br O CI Br OH OH 111 Br .!!!/Br F OH and ...m Br Br OH CI Br OH ་་་་་" ། ་arrow_forwardConsidering only rotation around the 1-2 bond, how many differentstaggered conformations are there of 1,2-dibromo-1,2-dichloropropane?A: 2; B. 3; C. 4; D. 6; E. more than 6.arrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285869759/9781285869759_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285199047/9781285199047_smallCoverImage.gif)