Write the state of hybridisation of boron in BF3.
SP2
Elements X, Y and Z have 4, 5 and 7 valence electrons respectively, (i) Write the molecular formula of the compounds formed by these elements individually with hydrogen, (ii) Which of these compounds will have the highest dipole moment?
Which of the following statements are not correct?
(a) NaCl being an ionic compound is a good conductor of electricity in the solid state.
(b) In canonical structures there is a difference in the arrangement of atoms.
(c) Hybrid orbitals form stronger bonds than pure orbitals.
(d) VSEPR theory can explain the square planar geometry of XeF4.
Assertion (A): Though the central atom of both NH3 and H20 molecules are sp3 hybridised, yet H – N – H bond angle is greater than that of H – O – H.
Reason (R): This is because nitrogen atom has one lone pair and oxygen atom has two lone pairs.
(a) A and R both are correct, and R is the correct explanation of A.
(b) A and R both are correct, but R is not the correct explanation of A.
(c) A is true but R is false.
(d) A and R both are false.
Although both CO2 and H2O are triatomic molecules, the shape of H2O molecule is bent while that of CO2 is linear. Explain this on the basis of dipole moment.
The skeletal structure of CH3COOH as shown below is correct, but some of the bonds are shown incorrectly. Write the correct Lewis structure for acetic acid.
Name the two conditions which must be satisfied for hydrogen bonding to take place in a molecule.
Is there any change in the hybridisation ofB and N atoms as a result of the following reaction ? BF3 + NH3 ——-> F3 B.NH3
Arrange the following bonds ‘in order of increasing ionic character giving reason.
N-H, F-H, C-H and O-H
Assertion (A): Among the two O – H bonds in H20 molecule, the energy required to break the first O – H bond and other O – H bond is the same.
Reason (R): This is because the electronic environment around oxygen is the same even after breakage of one O – H bond.
(a) A and R both are correct, and R is the correct explanation of A.
(b) A and R both are correct, but R is not the correct explanation of A.
(c) A is true but R is false.
(d) A and R both are false.
Write the important conditions required for the linear combination of atomic orbitals to form molecular orbitals.
Why does type of overlap given in the following figure not result in the bond formation?
Explain why CO2-3 ion cannot be represented by a single Lewis structure. How can it be best represented?
Which of the following statements are correct about CO32- ?
(a) The hybridization of central atom is sp3.
(b) Its resonance structure has one C – O single bond and two C = O double bonds.
(c) The average formal charge on each oxygen atom is 0.67 units.
(d) All C – O bond lengths are equal.
What is an ionic bond? With two suitable examples explain the difference between an ionic and covalent bond?
What is meant by the term average bond enthalpy? Why there is difference in bond enthalpy of O – H bond in ethanol (C2H5OH) and water?
Match the items given in Column I with examples given in Column II.
| Column I | Column II |
| (i) Hydrogen bond | (a) C |
| (ii) Resonance | (b) LiF |
| (iii) Ionic solid | (c) H2 |
| (iv) Covalent solid | (d) HF |
| (e) 03 |
Apart from tetrahedral geometry, another possible geometry for CH4 is square planar with the four H atoms at the comers of the square and the C atom at its centre. Explain why CH4 is not square planar?
(a) How many a and n bonds are present in
(b) Why Hf is more stable than H2?
(c) Why is B2 molecule paramagnetic?
In N0–3 ion, the number of bond pairs and lone pairs of electrons on nitrogen atom are
(a) 2, 2 (b) 3, 1 (c) 1,3 (d) 4, 0
Using molecular orbital theory, compare the bond energy and magnetic character of 0+2 and O–2
Write Lewis structure of the following compounds and show formal charge on each atom. HN03, No2, H2so4
The energy of σ2pz: molecular orbital is greater than 2px and 2pv molecular orbitals in nitrogen molecule. Write the complete sequence of energy levels in the increasing order of energy in the molecule. Compare the relative stability and the magnetic behaviour of the following species:
N2, N+2, N–2, N22+
