Concept explainers
Interpretation: In order to determine whether a ligand is a strong or weak-field ligand, whether octahedral Ni2+ or Cr2+ complex is used needs to be determined. The other method which can be used to check the relative ligand field strengths needs to be determined.
Concept Introduction:
Crystal field theory is the theory given to explain the bonding in the coordination complexes. As ligand approaches towards the metal ion, the d-orbital of metal ion divide according to the energy of metal ion. On the basis of energy and degeneracy, the d-orbital can be classified as
The spectrochemical series can be defined as the series of ligands in order of their ability of splitting the d-orbitals.
It can be used to study the light absorbed by the complexes as it shows the ligands from strong field to weak field.

Want to see the full answer?
Check out a sample textbook solution
Chapter 19 Solutions
Chemical Principles
- What chemical has the common name "lye"? Pick one of the 3 esters and show the hydrolysis mechanism to make a carboxylic acid. The organic “R” should be used to limit the redrawing time of the entire molecule. * see imagearrow_forwardProvide the products for each reaction. There are two and they are not related. *see imagearrow_forwardd. a phenylal Give the major organic product(s) of each of the following reactions or sequences of reactions. Show all levant stereochemistry. [three only] 0 A. B. CH3 Bra CH3COOH OH 1. Br₂, PBrz 2 H₂O 12arrow_forward
- 2arrow_forwardShow how the following conversions might be accomplished. Show all reagents and all intermediate ructures. More than one step may be required [2 ONLY]: A. B. ° C. OH 0 OH 0arrow_forwardA 20.3 mL sample of 0.263 M triethylamine, (C2H5)3N, is titrated with 0.252 M hydrochloric acid. (1) At the titration midpoint, the pH is . (2) At the equivalence point, the pH is .arrow_forward
- d. 3,4,5-trimethoxybenzoyl chloride . What is the order of decreasing reactivity towards nucleophilic acyl substitution for the arboxylic acid derivatives? (most reactive first) A. B. 0 0 O 0 0 H3C-C-O-C-CH3 H3C-C-N(CH3)2 H3C-C-OCH 3 (CH3)2CH-C-OCH3 I || ။ IV a. I, II, III, IV b. I, III, IV, II C. II, IV, III, I d. II, I, III, IV 0 0 0 0 0 R-C-O C-R R-C-NH2 R-C OR R-C-CI a. I, III, II, IV | 11 III IV b. II, III, I, IV c. III, II, I, IV d. IV, I, III, IIarrow_forwardB. d. a hydrate 4. Give the major organic product(s) for each of the following reactions or sequences of reactions. Show all relevant stereochemistry [4 ONLY]. A. CH₂OH PCC CH2Cl2 0 H KCN HCN 2arrow_forwardPropose a synthesis of the anti-inflammatory drug Ibuprofen from benzene. Show all reagents and all intermediate structures. Assume that ortho and para isomers can be separated. (CH3)2CHCH2 CH3 CHCOOH 1buprofen be requiredarrow_forward
- Assuming that no equilibria other than dissolution are involved, calculate the molar solubility of each of the following from its solubility product: (a) KHC4H4O6arrow_forwardAnswer the following by equation 1. reactio of CH3MgBr with Acetone [CH3COCH3] 2. acetal formation reaction of acetaldehyde [CH3CHO] 3. preparation of ethylmethylether [C2H5OCH3] 4. the acidity of the carboxylic acid depends and affected by the substitutions on the rest of the acid molecule: draw 2 structures of acids to show the different effects on acidity by different subsarrow_forwardConsider the reaction sequence below to answer the following questions: 0 0 0 0 0 1. NaOEt, EtOH H3O* OEt OET 2 PhCH Br heat Ph + EtOH + CO₂ CHh B C A A. The starting material A in this reaction sequence is called a a. ẞ-keto ester b. a-carboethoxy ketone C. malonic ester d. acetoacetic ester B. Conversion of A into B is a type of reaction termed a. an acylation b. an enolation C. d. an alkylation a phenylation f reactionsarrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistry: An Atoms First ApproachChemistryISBN:9781305079243Author:Steven S. Zumdahl, Susan A. ZumdahlPublisher:Cengage Learning
- Chemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningChemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistry: Principles and PracticeChemistryISBN:9780534420123Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward MercerPublisher:Cengage Learning





