Compare and comment on the difference in the single-bond energies for the elements of the second and third period of the following groups: group 14: C−C > Si−Si; but in Group 15: N−N < P−P; in Group 16: O−O <S-S and in group 17: F−F <Cl−Cl.
"C-C\t\\quad346kJ\/mol\\\\\nSi-Si\t\\quad222kJ\/mol\\\\\n\\quad\\\\\nN-N \\quad166kJ\/mol\\\\\nP-P\\quad201kJ\/mol\\\\\n\\quad\\\\\nO-O \\quad142kJ\/mol\\\\\nS-S \\quad226kJ\/mol\\\\\n\\quad\\\\\nf-f \\quad155kJ\/mol\\\\\nCl-Cl \\quad240kJ\/mol\\\\"
The bond energy for a C-C bond is slightly greater than the Si-Si bond. This difference is reflected in the chemistry of silicon versus carbon compounds. The chemistry of carbon is dominated by catenation: the ability of a chemical element to form a long chain-like structure via a series of covalent bonds. Although silicon does form Si-Si bonds, they are far more reactive than their C-C analogues, and polymers of silicon are predominantly comprised of Si-O chains (as a result of the very strong bond).
P-P single bonds are stronger than N-N single bonds because phosphorus (EN = 2.19) is much less electronegative than nitrogen (EN = 3.04). Also, phosphorus can expand its valence shell to hold more than eight electrons, but nitrogen cannot.
O−O bonds are much weaker than S-S bonds because Sulphur is less electronegative and has access to d orbitals.
F−F bonds are much less weaker than Cl−Cl bonds due to screening effect of the fluorine atom"."
Comments
Leave a comment