
Concept explainers
(a)
Interpretation:
The structure of the chelate complex [Pt (ox) 2]2- needs to be drawn.
Concept introduction:
Chelation is the process of bonding metal ion to other molecules and ions. The central atom is linked with two or more polydentate ligands by coordination bonds. These are called as chelates. The oxalate ion is a bidentate ligand having four oxygen atoms with lone pairs.
(b)
Interpretation:
The structure of the chelate complex [Cr (ox) 3]3- needs to be drawn.
Concept introduction:
Chelation is the process of bonding metal ion to other molecules and ions. The central atom is linked with two or more polydentate ligands by coordination bonds. These are called as chelates. The oxalate ion is a bidentate ligand having four oxygen atoms with lone pairs.
(c)
Interpretation:
The structure of the chelate complex [Fe (EDTA)] 2- needs to be drawn.
Concept introduction:
Chelation is the process of bonding metal ion to other molecules and ions. The central atom is linked with two or more polydentate ligands by coordination bonds. These are called as chelates. There are many agents and oxalates is one of them. The oxalate ion is a bidentate ligand having four oxygen atoms with lone pairs.

Want to see the full answer?
Check out a sample textbook solution
Chapter 24 Solutions
General Chemistry: Principles and Modern Applications, Loose Leaf Version (11th Edition)
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forward
- Synthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forward
- Indicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forward
- Question 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are reacted with sodium ethoxide in ethanol.arrow_forward
- Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage LearningChemistryChemistryISBN: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 & Chemical ReactivityChemistryISBN:9781337399074Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage LearningChemistry & Chemical ReactivityChemistryISBN:9781133949640Author:John C. Kotz, Paul M. Treichel, John Townsend, David TreichelPublisher:Cengage Learning





