Part A. 1. Write equations to describe what happened when: a. Carbon dioxide was dissolved in water. co2(g) + H2O() <-> H2CO3(aq) <--> HC03-(aq) + H3O+(aq) b. When the indicator bromothymol blue was added to cold water. Hin(aq) + H20() <-> H3O+(aq) + In-(aq) C. From equations la and lb above, when NaOH was added to flasks A and B, why did the indicator initially turn blue? Explain your answer in terms of the equilibrium of equation 1b. Then you left the two flasks to stand for several minutes after the addition of NaOH, why did the contents of flask A again change colour back from blue to yellow? Explain your answer in terms of the equilibrium in lb above. The time delay for the second colour change back to yellow implies that the overall speed of the two-step conversion of carbon dioxide shown as equation (8) on page D7 is slow. Which is the slow step? Explain the basis of your answer.
Basics in Organic Reactions Mechanisms
In organic chemistry, the mechanism of an organic reaction is defined as a complete step-by-step explanation of how a reaction of organic compounds happens. A completely detailed mechanism would relate the first structure of the reactants with the last structure of the products and would represent changes in structure and energy all through the reaction step.
Heterolytic Bond Breaking
Heterolytic bond breaking is also known as heterolysis or heterolytic fission or ionic fission. It is defined as breaking of a covalent bond between two different atoms in which one atom gains both of the shared pair of electrons. The atom that gains both electrons is more electronegative than the other atom in covalent bond. The energy needed for heterolytic fission is called as heterolytic bond dissociation energy.
Polar Aprotic Solvent
Solvents that are chemically polar in nature and are not capable of hydrogen bonding (implying that a hydrogen atom directly linked with an electronegative atom is not found) are referred to as polar aprotic solvents. Some commonly used polar aprotic solvents are acetone, DMF, acetonitrile, DMSO, etc.
Oxygen Nucleophiles
Oxygen being an electron rich species with a lone pair electron, can act as a good nucleophile. Typically, oxygen nucleophiles can be found in these compounds- water, hydroxides and alcohols.
Carbon Nucleophiles
We are aware that carbon belongs to group IV and hence does not possess any lone pair of electrons. Implying that neutral carbon is not a nucleophile then how is carbon going to be nucleophilic? The answer to this is that when a carbon atom is attached to a metal (can be seen in the case of organometallic compounds), the metal atom develops a partial positive charge and carbon develops a partial negative charge, hence making carbon nucleophilic.
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