<span>All metals have similar properties BUT, there can be wide variations in melting point, boiling point, density, electrical conductivity and physical strength.<span>To explain the physical properties of metals like iron or sodium we need a more sophisticated picture than a simple particle model of atoms all lined up in close packed rows and layers, though this picture is correctly described as another example of a giant lattice held together by metallic bonding.</span><span>A giant metallic lattice – the <span>crystal lattice of metals consists of ions (NOT atoms) </span>surrounded by a 'sea of electrons' that form the giant lattice (2D diagram above right).</span><span>The outer electrons (–) from the original metal atoms are free to move around between the positive metal ions formed (+).</span><span>These 'free' or 'delocalised' electrons from the outer shell of the metal atoms are the 'electronic glue' holding the particles together.</span><span>There is a strong electrical force of attraction between these <span>free electrons </span>(mobile electrons or 'sea' of delocalised electrons)<span> (–)</span> and the 'immobile' positive metal ions (+) that form the giant lattice and this is the metallic bond. The attractive force acts in all directions.</span><span>Metallic bonding is not directional like covalent bonding, it is like ionic bonding in the sense that the force of attraction between the positive metal ions and the mobile electrons acts in every direction about the fixed (immobile) metal ions of the metal crystal lattice, but in ionic lattices none of the ions are mobile. a big difference between a metal bond and an ionic bond.</span><span>Metals can become weakened when repeatedly stressed and strained.<span><span>This can lead to faults developing in the metal structure called 'metal fatigue' or 'stress fractures'.</span><span>If the metal fatigue is significant it can lead to the collapse of a metal structure.</span></span></span></span>
The alkali metals are so reactive that they are never found in nature in elemental form. Although some of their ores are abundant, isolating them from their ores is somewhat difficult. For these reasons, the group 1 elements were unknown until the early 19th century, when Sir Humphry Davy first prepared sodium (Na) and potassium (K) by passing an electric current through molten alkalis. (The ashes produced by the combustion of wood are largely composed of potassium and sodium carbonate.) Lithium (Li) was discovered 10 years later when the Swedish chemist Johan Arfwedson was studying the composition of a new Brazilian mineral. Cesium (Cs) and rubidium (Rb) were not discovered until the 1860s, when Robert Bunsen conducted a systematic search for new elements. Known to chemistry students as the inventor of the Bunsen burner, Bunsen’s spectroscopic studies of ores showed sky blue and deep red emission lines that he attributed to two new elements, Cs and Rb, respectively. Francium (Fr) is found in only trace amounts in nature, so our knowledge of its chemistry is limited. All the isotopes of Fr have very short half-lives, in contrast to the other elements in group 1.
Lithium heparin tube i think, could be wrong but i think this is right.
Answer:
D. [NO₂]²/[N₂O₄]
Explanation:
The equilibrium constant expression for a reaction is products over reactants. Since NO₂ has a coefficient of 2, it will become an exponent.
So, it would be:
[NO₂]²/[N₂O₄]
Hope that helps.
