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Specify the coordination geometry around and hybridization of N and B atoms in a 1:1 complex of BF3 and NH3:

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Explanation

(a) No doubt NH3 and BF3 have sp3 (pyramidal) and sp2 (coplanar) hybridization respectively having one lone pair of electron on N atom which is responsible for pyramidal shape of NH3 inspite of sp3 hybridization. However, as soon as it is coordinated to BF3,  both attain tetrahedral geometry and acquire sp3- hybridization.  

When O2 is adsorbed on a metallic surface, electron transfer occurs from the ,metal to O2. The wrong statements(s) regarding this adsorption is (are): 

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Explanation

 (a)

(a) :Incorrect : Because electronic transfer takes place and it is chemisorbtion.

(b) :correct: Adsorbtion is always exothermic.

(c) :correct: O2 will accept the electron from metal into its π*2p orbital.

(d) :correct: Since the electron enters into π* orbital bond order decrease  and bond length increases.

The BF3 is a planarn molecule where as NF3 is pyramidal because:

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Explanation

The BF3 molecule has a planar structure due to the absence of lone pairs on the central boron atom. In contrast, the NF3 molecule adopts a pyramidal structure because the nitrogen atom has one lone pair of electrons, causing repulsion and distorting the molecular geometry.

Which of the following statement is true for IO2F2-according to VSEPR theory?

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Explanation

According to VSEPR theory, the IO2F2- ion has a trigonal bipyramidal structure with the two lone pairs and two I-O double bonds occupying the equatorial positions, which is analogous to the structure of SF4. Therefore, both options (A) and (C) are correct.

In the structure of H2CSF4, to decide the plane in which C = S is present the following bond angle value are given

Axial FSF angle idealised=180°                     170°

Equatorial FSF angle idealised=120°               97°

After deciding the plane of double bond, which of the following statements is correct?

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According to Molecular orbital theory which of the following statement is incorrect?

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Explanation

c. 

(A), (B) M.O. for C2σ1s2<σ1*s2<σ2s2<σ2*s2<π2p2y=π2p2zHOMO<σ2pxLUMO, two π molecular orbitals are involved in bonding .

(C) It is isoelectronic with N2 and has one sigma and two pie-bonds.

(c) In both, all electrons are paired so diamagnetic.

A diatomic molecule has a dipole moment of 1.2 D. If its bond length is equal to 10 -10 m then the fraction of an electronic charge on each atom will be:

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Explanation

(D) μ=q×d

1.2×10-18=q×10-8cm

q=1.2×10-1810-8=1.2×10-10%charge =qe×=1.2×10-104.8×10-10×100=25%

Which of the following statements is correct?

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Explanation

All the given statements are correct. (CH3)3COH is less acidic than (CH3)3SiOH due to the poorer ability of silicon to stabilize the negative charge on the conjugate base. CO is a stable molecule, but its silicon analogue is not stable. In phosgene (COCl2), the C-O bond length is longer than expected due to the presence of resonance, while the C-Cl bond length is shorter.

The increasing order of the strength of hydrogen bond in the following mentioned linkages
is

(i) O — H — S     (ii) O — H  — O    (iii) F – H – F   (iv) F – H – O

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Explanation

(A) Strength of H-bonds on following factors.
      (i) Electronegativity of element covalently bonded to hydrogen atom.
      (ii) Size of electronegative element.
      (iii) Ease of donation of lone pair of electrons by electronegative element.

The boiling pot of CCl4 is higher than that of CHCl3 because :

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Explanation

(C)  Number of polarisable electrons  strength of vander waal’s force  boiling point.
       boiling point CHCl3=61°C and CCl4=73°C.

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