![GEN COMBO CHEMISTRY: ATOMS FIRST; ALEKS 360 2S ACCESS CARD CHEMISTRY:ATOMS FIRST](https://www.bartleby.com/isbn_cover_images/9781260020229/9781260020229_smallCoverImage.jpg)
Concept explainers
Rank the following ions in order of increasing number of unpaired electrons: Tr3+, Fe2+, V3+, Cu+, Mn4+.
![Check Mark](/static/check-mark.png)
Interpretation: It should be ranked the given set of ions in increasing order of number of unpaired electrons.
Concept Introduction:
- Aufbau Principle tells that the orbital with the lower energy is filled with electrons first and then the filling of higher energy orbital follows. By using this, valence orbital diagram can be draw for any atoms or ions.
- Electronic configuration is the arrangement of the electrons of atoms in the orbital. The electronic configurations are writing for atoms and ions, in accordance with Pauli Exclusion Principle and Hund’s rule.
- According to Pauli Exclusion Principle, no two electrons having the same spin can occupy the same orbital.
- According to Hund’s rule, the orbital in the subshell is filled singly by one electron before the same orbital is doubly filled. When the orbital is singly filled, all the electrons have same spin. In a doubly filled orbital, there are two electrons with opposite spin.
To determine the increasing order of unpaired electrons present in the given set of ions.
Answer to Problem 4.79QP
Ions in increasing order of unpaired electrons,
Explanation of Solution
Electronic configuration of
The valence orbital diagram of
The electronic configuration of
Electronic configuration of
The electronic configuration of
The valence orbital diagram is drawn as shown above. From this, we can find that there is one unpaired electron and which is highlighted in red colour.
Electronic configuration of
The electronic configuration of
Electronic configuration of
The electronic configuration of
The valence orbital diagram is drawn as shown above. From this, we can find that there are four unpaired electrons that are highlighted in red colour.
Electronic configuration of
The electronic configuration of
Electronic configuration of
The electronic configuration of
The valence orbital diagram is drawn as shown above. From this, we can find that there are two unpaired electrons, that are highlighted in red colour.
Electronic configuration of
The electronic configuration of
Electronic configuration of
The electronic configuration of
The valence orbital diagram is drawn as shown above. From this we can find that there are no unpaired electrons present.
Electronic configuration of
The electronic configuration of
Electronic configuration of
The electronic configuration of
The valence orbital diagram is drawn as shown above. From this, we can find that there are three unpaired electrons present and the same is highlighted in red colour.
Given ions were ranked in increasing order of unpaired electron as follows,
From the number of unpaired electrons for each of the given ions found out in the previous steps we can arrange them in increasing order of number of unpaired electrons as shown above.
The given sets of ions were ranked in increasing order of number of unpaired electrons.
Want to see more full solutions like this?
Chapter 4 Solutions
GEN COMBO CHEMISTRY: ATOMS FIRST; ALEKS 360 2S ACCESS CARD CHEMISTRY:ATOMS FIRST
- 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
- Chemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage LearningGeneral Chemistry - Standalone book (MindTap Cour...ChemistryISBN:9781305580343Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; DarrellPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9780534420123/9780534420123_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305580343/9781305580343_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781133949640/9781133949640_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781285199047/9781285199047_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781337399074/9781337399074_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)