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find oxidation no of Fe in Fe4[Fe(CN)6]3
CH3CH2NO2 will show
a)position isomerism
b)functional isomerism
c)tautomerism
d)geometrical isomerism
and why?
What is the seris of IRVING WILLIAM STABILITY ORDER........
Name the compound [Zn (NH3)4]2+.
IUPAC Name of
LiAlH4
what do u mean by "primary valency is ionisable"??
The state of hybridisation of central atom of anoinic part of solid PBr5 is.....
AgCl dissolves in NH4OH due to formation of...............
EXPLAIN???
what is the hybridisation of Pt(NH3)6Cl4
Please give list of all exceptional cases in hybridisation
in which there is outer orbital hybridisation....
why does [CoCl4]2- show dsp2 hybridization instead of sp3?
what are inner d orbitals and outer d orbitals?
CoCl3.4NH3, respectively, is what is secondary valency in this case
How is this compound to be named?
Please show the calculation for the oxidation number
[Pt(NH3)2Cl(NH2CH3)]Cl
EAN of copper in cuprammonium sulphate is:
is C2O4(2-) a weak ligand or strong ligand?
if z is no. of atoms in unit cell that represents closest packing sequence ABC ABC . then what is no of tetrahedral voids in unit cell equal to?
How to find oxidation no of Ag in [(NH3)2] [Ag(CN)2]
How many geometrical isomers are there in the complex, [Pt(Py)(NH3)BrCl] ? Even show the process.
how can we find whether the given coordinate compound is paramagnatic or dimagnetic in nature?what are the other factors on which magnetic properties depends?
How to decide whether a compound will show optical isomerism
In coordination compounds
How is colour of coordination entity determined from complementary colour absorbed?
Is (CoCl3(H2O)3).3H2O hydrate isomer of CoCl3.6H2O PLEASE EXPLAIN....
how to do nomenclature of bridged cordination compounds
[Ag(NH3)2][Ag(CN)2] is named as:
dear expert in the study material of coordination u have given the concept of basic thing and in example u have given about optical isomerism, nomenclature how we r able to understand
1- i m unable to understand soln of this question
The ratio of moles of AgCl precipitated on adding AgNO3to PdCl2.4NH3and CoCl3.4NH3, respectively, is
plz make me clear and explain the answer step by step
2- i have doubt that no2 exist at neutral and +1 form i m unable to understand which i have to take while calculating the oxi no and ean explain the logic behind this
Q- this is given in ncert exampler - when 0.1 mol cocl3(nh3)5 is treated with excess of agno3 o.2 mole of agcl are obtained find conductivity
Q- MATCH THE FOLLOWING
column 2- violet, green, pale yellow, yellowish orange, blue
Q-
Foran octahedral complex, with P.E aprox. to 0 d6 electronic configuration of central metal ion in presence of strong field ligand , find incorrect ststement (s) regarding crystal field stablisation energy (CFSE) spiliting energy {(delta not)[/0]}
(a)[CFSE] will be = to spilting energy /0
(b)[CFSE] will be than spilting energy /0
(c) [CFSE] will be
(d) Both [CFSE] spilting energy R same for each octahedral complex with any electronic configuration of central metal atom
how to calculate secondary valency and tell me while writing name of complex compounds for eg k4[Fe(CN)6] why we cant write tetrapotassium hexacyanoferrate(II) instead we write potassium hexacyanoferrate(II) please explain me
how can a square planar complex of MABCD type show trans isomerism (M = metal A, B, C, D = LIGANDS)?
coordination number of Fe in oxyhaemoglobin is ?
What is primary and secondary valency in coordination compounds? Please explain conceptually with example
1- i think in mn 3 plus only1 d is vecant hybridisation is dsp3
2-justify this vbt doesnt make exact prediction regarding the tetrahedral and square planer str of 4- coordinated complex
3- justify and explain d orbitals splitting is inverted and is smaller as compare to octahedral field splitting
4- how dd transition helps in deciding the colour of complex
5- explain instability constant and compile complex
ligand in a complex salt are..
please explain it also...
see by urself how much delaying
State all the possible value for n in dn configuration the no of u.p e in octahedral complex remain same irrespective of the lig field strength
A d block elements forms octahedral complex but its mu remains same either in sfl or wfl state the conf for d d1,d2.... upto d10 which is best suitable for this is it always form coloured cpd and is no of e in t2g is lower then eg orbitals explain all these things in better way
Asked byKeshav Kr3 weeks agoSubject:Chemistry
Asked byKeshav Kr5 days, 15 hours agoSubject:Chemistry
EAN of Fe in K4Fe(CN)6 Explain the procedure
E.g: 9876543210, 01112345678
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Syllabus
find oxidation no of Fe in Fe4[Fe(CN)6]3
CH3CH2NO2 will show
a)position isomerism
b)functional isomerism
c)tautomerism
d)geometrical isomerism
and why?
What is the seris of IRVING WILLIAM STABILITY ORDER........
Name the compound [Zn (NH3)4]2+.
a. [Co(NH3)6]Cl3 b.K4[Fe(CN)6] c. K2[PtCl4] d.[Cr(NH3)3Cl3]
IUPAC Name of
LiAlH4
(1) [Fe(CO)]-5
(2) [Ni(CO)4]
what do u mean by "primary valency is ionisable"??
The state of hybridisation of central atom of anoinic part of solid PBr5 is.....
AgCl dissolves in NH4OH due to formation of...............
EXPLAIN???
what is the hybridisation of Pt(NH3)6Cl4
Please give list of all exceptional cases in hybridisation
in which there is outer orbital hybridisation....
why does [CoCl4]2- show dsp2 hybridization instead of sp3?
what are inner d orbitals and outer d orbitals?
CoCl3.4NH3, respectively, is what is secondary valency in this case
How is this compound to be named?
Please show the calculation for the oxidation number
[Pt(NH3)2Cl(NH2CH3)]Cl
EAN of copper in cuprammonium sulphate is:
is C2O4(2-) a weak ligand or strong ligand?
if z is no. of atoms in unit cell that represents closest packing sequence ABC ABC . then what is no of tetrahedral voids in unit cell equal to?
How to find oxidation no of Ag in [(NH3)2] [Ag(CN)2]
How many geometrical isomers are there in the complex, [Pt(Py)(NH3)BrCl] ? Even show the process.
how can we find whether the given coordinate compound is paramagnatic or dimagnetic in nature?what are the other factors on which magnetic properties depends?
How to decide whether a compound will show optical isomerism
In coordination compounds
How is colour of coordination entity determined from complementary colour absorbed?
Is (CoCl3(H2O)3).3H2O hydrate isomer of CoCl3.6H2O PLEASE EXPLAIN....
how to do nomenclature of bridged cordination compounds
low spin complex of d6 -cation in an octahedral field will have what energy
[Ag(NH3)2][Ag(CN)2] is named as:
diamminesilver(I) dicyanoargentate(I)please explain me,why it is named as this,and why the name of central atom differ since both are Ag.dear expert in the study material of coordination u have given the concept of basic thing and in example u have given about optical isomerism, nomenclature how we r able to understand
1- i m unable to understand soln of this question
The ratio of moles of AgCl precipitated on adding AgNO3to PdCl2.4NH3and CoCl3.4NH3, respectively, is
plz make me clear and explain the answer step by step
2- i have doubt that no2 exist at neutral and +1 form i m unable to understand which i have to take while calculating the oxi no and ean explain the logic behind this
Q- this is given in ncert exampler - when 0.1 mol cocl3(nh3)5 is treated with excess of agno3 o.2 mole of agcl are obtained find conductivity
Q- MATCH THE FOLLOWING
column 2- violet, green, pale yellow, yellowish orange, blue
Q-
Foran octahedral complex, with P.E aprox. to 0 d6 electronic configuration of central metal ion in presence of strong field ligand , find incorrect ststement (s) regarding crystal field stablisation energy (CFSE) spiliting energy {(delta not)[/0]}
(a)[CFSE] will be = to spilting energy /0
(b)[CFSE] will be than spilting energy /0
(c) [CFSE] will be
(d) Both [CFSE] spilting energy R same for each octahedral complex with any electronic configuration of central metal atom
Thank you.
how to calculate secondary valency and tell me while writing name of complex compounds for eg k4[Fe(CN)6] why we cant write tetrapotassium hexacyanoferrate(II) instead we write potassium hexacyanoferrate(II) please explain me
how can a square planar complex of MABCD type show trans isomerism (M = metal A, B, C, D = LIGANDS)?
1)Na2[Cr edta]
2)[Co(NO2)2(C5H5n)2(NH3)2]NO3
3)[Pd I2(ONO)2(H2O)2]
4)Hg[CO(CNS)4]
5)Cr[(PPH)3(CO5)]
6)[Cr NCS (NH3)5][ZnCl4]
7)[CoCl2(NH3)4]3[Cr(CN)6]
8)K2[HgI4]
9)[Co Cl ONO(en)2]+
10) [Cr(H2O)5SCN]
11)Cs[FeCl4]
12)K4[Mn(CN)6]
13)K[(H2O)2(C2O4)2].3H2O
coordination number of Fe in oxyhaemoglobin is ?
What is primary and secondary valency in coordination compounds? Please explain conceptually with example
1- i think in mn 3 plus only1 d is vecant hybridisation is dsp3
2-justify this vbt doesnt make exact prediction regarding the tetrahedral and square planer str of 4- coordinated complex
3- justify and explain d orbitals splitting is inverted and is smaller as compare to octahedral field splitting
4- how dd transition helps in deciding the colour of complex
5- explain instability constant and compile complex
Please explain.
Thank you.
ligand in a complex salt are..
please explain it also...
OPTIONS : A) 8 B) 10 C) 12 D) 14
see by urself how much delaying
State all the possible value for n in dn configuration the no of u.p e in octahedral complex remain same irrespective of the lig field strength
A d block elements forms octahedral complex but its mu remains same either in sfl or wfl state the conf for d d1,d2.... upto d10 which is best suitable for this is it always form coloured cpd and is no of e in t2g is lower then eg orbitals explain all these things in better way
Asked byKeshav Kr3 weeks agoSubject:Chemistry
Asked byKeshav Kr5 days, 15 hours agoSubject:Chemistry
EAN of Fe in K4Fe(CN)6 Explain the procedure
i did not unerstand the answer that was given in the site
sir can you please explain