BURDGE CHEMISTRY VALUE ED (LL)
4th Edition
ISBN: 9781259995958
Author: VALUE EDITION
Publisher: MCG CUSTOM
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Question
Chapter 22, Problem 13QP
Interpretation Introduction
Interpretation:
The oxidation number of the metal in the given compoundis to be determined.
Concept introduction:
Coordination compounds are the compounds formed by the reaction of metal ions with polar molecules, or with a group of anions. They contain coordinate covalent bonds.
Oxidation number is also called the oxidation state. It is used to describe the oxidation, that is, theloss of electrons, in any compound.
The overall charge can be calculated by adding the total charge on the complex.
Alkali metal cation (sodium) has charge +1
Cyanide ligands have a negative charge of
Oxygen has a charge of
Magnesium having oxidation number
Carbonyl group is a neutral ligand, haszero charge.
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Students have asked these similar questions
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
×
NO2
○ donating
O donating
O withdrawing
O withdrawing
O electron-rich
electron-deficient
no inductive effects
O no resonance effects
O similar to benzene
E
[
CI
O donating
withdrawing
O no inductive effects
Explanation
Check
○ donating
withdrawing
no resonance effects
electron-rich
electron-deficient
O similar to benzene
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Understanding how substituents activate
Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic
aromatic substitution.
Explanation
HN
NH2
Check
X
(Choose one)
(Choose one)
(Choose one)
(Choose one)
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Identifying electron-donating and electron-withdrawing effects on benzene
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.
Inductive Effects
Resonance Effects
Overall Electron-Density
Molecule
CF3
O donating
O donating
O withdrawing
O withdrawing
O no inductive effects
O no resonance effects
electron-rich
electron-deficient
O similar to benzene
CH3
O donating
O withdrawing
O no inductive effects
O donating
O withdrawing
Ono resonance effects
O electron-rich
O electron-deficient
O similar to benzene
Explanation
Check
Х
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Chapter 22 Solutions
BURDGE CHEMISTRY VALUE ED (LL)
Ch. 22.1 - Prob. 1PPACh. 22.1 - Prob. 1PPBCh. 22.1 - Prob. 1PPCCh. 22.1 - Prob. 1CPCh. 22.1 - Prob. 2CPCh. 22.1 - Prob. 3CPCh. 22.1 - Prob. 4CPCh. 22.2 - Prob. 1PPACh. 22.2 - Prob. 1PPBCh. 22.2 - Prob. 1PPC
Ch. 22.3 - Prob. 1PPACh. 22.3 - Prob. 1PPBCh. 22.3 - Prob. 1PPCCh. 22.3 - Prob. 1CPCh. 22.3 - Prob. 2CPCh. 22.4 - Prob. 1PPACh. 22.4 - Practice Problem BUILD
Transition metal ions can...Ch. 22.4 - Prob. 1PPCCh. 22 - Prob. 1QPCh. 22 - Prob. 2QPCh. 22 - 22.3 Explain why atomic radii decrease very...Ch. 22 - Prob. 4QPCh. 22 - Write the electron configurations of the following...Ch. 22 - Prob. 6QPCh. 22 - Prob. 7QPCh. 22 - Prob. 8QPCh. 22 - Describe the interaction between a donor atom and...Ch. 22 - Prob. 10QPCh. 22 - Complete the following statements for the complex...Ch. 22 - Prob. 12QPCh. 22 - Prob. 13QPCh. 22 - Prob. 14QPCh. 22 - Prob. 15QPCh. 22 - Prob. 16QPCh. 22 - Prob. 17QPCh. 22 - Prob. 18QPCh. 22 - Prob. 19QPCh. 22 - Prob. 20QPCh. 22 - Prob. 21QPCh. 22 - The complex ion [Ni ( CN ) 2 Br 2 ] 2- has a...Ch. 22 - Prob. 23QPCh. 22 - Prob. 24QPCh. 22 - Prob. 25QPCh. 22 - Prob. 26QPCh. 22 - Prob. 27QPCh. 22 - Prob. 28QPCh. 22 - Prob. 29QPCh. 22 - Prob. 30QPCh. 22 - Prob. 31QPCh. 22 - Prob. 32QPCh. 22 - Prob. 33QPCh. 22 - Prob. 34QPCh. 22 - Prob. 35QPCh. 22 - Prob. 36QPCh. 22 - Prob. 37QPCh. 22 - Prob. 38QPCh. 22 - Prob. 39QPCh. 22 - Prob. 40QPCh. 22 - Prob. 41QPCh. 22 - A concentrated aqueous copper(II) chloride...Ch. 22 - Prob. 43QPCh. 22 - Prob. 44QPCh. 22 - Prob. 45APCh. 22 - Prob. 46APCh. 22 - Prob. 47APCh. 22 - Prob. 48APCh. 22 - Prob. 49APCh. 22 - Draw qualitative diagrams for the crystal held...Ch. 22 - Prob. 51APCh. 22 - Prob. 52APCh. 22 - Prob. 53APCh. 22 - Prob. 54APCh. 22 - Prob. 55APCh. 22 - Prob. 56APCh. 22 - Prob. 57APCh. 22 - Prob. 58APCh. 22 - 22.59 The -porphyrin complex is more stable than...Ch. 22 - Prob. 60APCh. 22 - Prob. 61APCh. 22 - Prob. 62APCh. 22 - Prob. 63APCh. 22 - Prob. 64APCh. 22 - Prob. 65APCh. 22 - Prob. 66APCh. 22 - Prob. 67APCh. 22 - Prob. 68APCh. 22 - Locate the transition metal atoms and ions in the...Ch. 22 - Prob. 70APCh. 22 - Prob. 71APCh. 22 - Copper is known to exist in the +3 oxidation...Ch. 22 - 22.73 Chemical analysis shows that hemoglobin...Ch. 22 - Prob. 74APCh. 22 - Prob. 75APCh. 22 - Prob. 76APCh. 22 - 22.77 Commercial silver-plating operations...Ch. 22 - Prob. 78APCh. 22 - 22.79 (a) The free Cu(I) ion is unstable in...Ch. 22 - Prob. 1SEPPCh. 22 - Prob. 2SEPPCh. 22 - Prob. 3SEPPCh. 22 - Prob. 4SEPP
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- 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 O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forwardIdentifying electron-donating and 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 NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_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 Х (Choose one) OH (Choose one) OCH3 (Choose one) OH (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward
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