Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes.
Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc.
Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes.
The hybridization of `[NiCl_(2)(PPh_(3))_(2)]" and "[NiCl_(2).(Pme_(3))_(2)]` are respectively (consider `PPh_(3)` a bulkier ligand than `Pme_(3)`) :
Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes.
Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc.
Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes.
The hybridization of `[NiCl_(2)(PPh_(3))_(2)]" and "[NiCl_(2).(Pme_(3))_(2)]` are respectively (consider `PPh_(3)` a bulkier ligand than `Pme_(3)`) :
Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc.
Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes.
The hybridization of `[NiCl_(2)(PPh_(3))_(2)]" and "[NiCl_(2).(Pme_(3))_(2)]` are respectively (consider `PPh_(3)` a bulkier ligand than `Pme_(3)`) :
A
`sp^(3)" and "dsp^(2)`
B
`sp^(3)" and "sp^(3)`
C
`dsp^(2)" and "dsp^(2)`
D
`dsp^(2)" and "sp^(3)`
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The correct Answer is:
A
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Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes. Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc. Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes. Which of the following is correct for the complex [Ti(H_(2)O)_(6)]^(3+) ?
Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes. Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc. Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes. Which of the following is correct for the complex [Ti(H_(2)O)_(6)]^(3+) ?
A
Hybridization of central metal ion of the complex is `sp^(3)d^(2)`.
B
The complex is paramagnetic containing one unpaired electron.
C
Hybridization of central metal ion of the complex is `d^(2)sp^(3)`.
D
Both (b) and (c ).
Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes. Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc. Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes. Which of the following is correct for the complex [Ti(H_(2)O)_(6)]^(3+) ?
Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes. Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc. Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes. Which of the following is correct for the complex [Ti(H_(2)O)_(6)]^(3+) ?
A
Hybridization of central metal ion of the complex is `sp^(3)d^(2)`.
B
The complex is paramagnetic containing one unpaired electron.
C
Hybridization of central metal ion of the complex is `d^(2)sp^(3)`.
D
Both (b) and (c ).
Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes. Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc. Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes. Select the correct statement about the crystal field theory.
Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes. Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc. Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes. Select the correct statement about the crystal field theory.
A
Metal-ligand bond in coordination compounds arises purely from electrostatic interaction between the metal ion and the ligand.
B
Metal-ligand bond in coordination compound is purely a covalent bond.
C
The pattern of splitting of the d-orbitals depends upon the nature of the cystal field.
D
Both (a) and (c ).
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Valence bond theory for bonding in transition metal complexes was developed by Pauling. From the valence bond point of view, formation of a complex involves reaction between Lewis bases (ligands) and a Lewis acid (metal atom or metal ion) with the formation of coordination covalent (or dative) bonds between them. The model utilizes hybridization of metal s, p and d valence orbitals to account for the observed structures and magnetic properies of complexes. Valence bond theory is able to deal satisfactorily with many stereo chemical and magnetic properies but is has nothing to say about electronic spectra or the reason for the kinetic inertness of chromium (III) and low spin cobalt (III) octahedral complexes. To understand this and more other features of transition metal we must turn to other theories like crystal field theory etc. Pure crystal field theory assumes that the only interaction between the metal ion and the ligands is an electrostatic or ionic one with the ligands being regarded as negative point charges. This theory is quite successful in interpreting many important properties of complexes. Select the correct statement about the crystal field theory.
Valence bond theory explains
Valence bond theory was introduced by
Which is not correct about valence bond theory of metals
A. According to C.FT complex compound contain point charges R: The bonding between central metal ion and ligand is electrostatic