The correct order of decreasing length of the bond as indicated by the arrow in the following structures is
I > II > III
II > I > III
III > II > I
I > III > II
C.
III > II > I
The length of carbon-carbon single bond is always greater than that of the carbon-carbon double bond.
In III, positive charge is not in conjugation of double bond, so the bond does not acquire a double bond character. However, chances of acquiring double bond character (of the indicated bond) is much more in I than that in case of II. Thus, the correct order of decreasing bond length is
In case of heteronuclear diatomics of the type AB, where A is more electronegative than B, bonding molecular orbital resembles the character of A more than that of B. The statement
is false
is true
cannot be evaluated since data is not sufficient
is true only for certain systems
Dipole-induced dipole interactions are present in which of the following pairs?
H2O and alcohol
Cl2 and CCl4
HCl and He atoms
SiF4 and He atoms
The bond angle in NF3 (102.3°) is, smaller than NH3 (107.2°). This is because of
large size of F compared to H
large size of N compared to F
opposite polarity of N in the two molecules
small size of H compared to N
The structure of XeF6 is experimentally determined to be distorted octahedron. Its structure according to VSEPR theory is
octahedron
trigonal bipyramid
pentagonal bipyramid
tetragonal bipyramid
In the following electron-dot structure calculate the formal charge from left to right nitrogen atom; :
-1 , -1 , +1
-1 , +1 , -1
+1 , -1 , -1
+1 , -1 , +1
The sp3d2 hybridisation of central atom of a molecule would lead to:
square planar geometry
tetrahedral geometry
trigonal bipyramidal geometry
octahedral geometry