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GROUP 14: TIN AND LEAD
Tin and lead give some resemblance to the lighter elements in group 14, especially Ge. Although they are uniquely more metallic in their physical and chemical characteristics, simple cationic chemistry is the exception rather than the rule. As with group 13, two oxidation states MIV and MII are found, the MII form giving more stable for lead.
Both substances have rather low abundance, but are commoner than other heavy metals. They occur in the minerals galena PbS and cassiterite SnO2. They each have various stable isotopes, Sn more than any other element (10). Some Pb isotopes are discovered from the radioactive decay of uranium and thorium. The isotopic composition of Pb (and thus its atomic mass) differs detectably according to the source, and such variations have been used to estimate the age the Earth of and of rocks.
The elements are readily made by reduction of their ores and are soft, low-melting, somewhat unreactive metals. Tin is required for plating, and both elements in low-melting alloys and as many elements. Applications of lead are declining as its substances are very toxic. A continuing major need is in leadacid batteries, which depend on two reactions involving the PbII, Pb0 and PbIV states:
Occurring at different electrodes, these show a cell potential of 2 V, greater than can be obtained easily from any other pair of electrode reactions in aqueous solution
Chloroform
perkin ring closure reaction of melonic ester with C2H5O-Na+
#question. CH3CH=CHCH +Br2 ___ .
The Ca 2+ and Mg 2+ ions in hard water form scum with soap. Therefore they don''t form lather and therefore don''t clean the dirt.
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the properties of s,p,d,f block elements?
Number of unpaired electrons in the ground state of beryllium atom is: (1) 2 (2) 1 (3) 0 (4) All the above Ans: 0
Suppose that lysine is dissolved into a buffer to a concluding concentration of 1 mM. Into this buffer, 80 percent of the lysine's side-chain amines are protonated. Determine the p
Reactions of Benzene Nucleus - Nitration Phenol reacts along with dilute nitric acid at 5-10°C to form ortho and para nitro phenols, although the yield is meager because of oxi
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