Answer:
Distillation will generate the most cyclohexene.
Explanation:
Let us assume following attached reaction for the synthesis of cyclohexene from cyclohexanol which attains equilibrium after certain time.
As shown in figure the cyclohexanol upon treatment with phosphoric acid undergoes dehydration reaction (removal of water) and produces cyclohexene. On the other hand cyclohexene reacts with water (hydration reaction) and produces cyclohexanol.
Now, if this reaction is allowed in a single flask it will attain equilibrium and will not generate the cyclohexene in high quantity. On the other hand if we apply <em>Le Chatelier's principle</em> ( <u><em>removal of product moves the equilibrium in right direction</em></u>) and distillate cyclohexene (boiling the cyclohexene to convert it into vapors and then collect it after condensation) will move the reaction in forward direction and will allow us to generate cyclohexene in high amounts.
Scale and measuring tape.
To determine the mass and volume, you can find the density. The block will float if its density is less than that of water.
Answer:
An acid is a substance that donates protons (in the Brønsted-Lowry definition) or accepts a pair of valence electrons to form a bond (in the Lewis definition). A base is a substance that can accept protons or donate a pair of valence electrons to form a bond.
Hope it helps!!!
Answer:
Experiments to determine mechanisms involve looking at indirect evidence to help support or disprove a proposed mechanism.
Most intermediates are not typically isolated to determine reaction mechanisms.
Carbocations are very reactive and are typically not isolated for analysis.
Scientists can prove that a specific mechanism exists.
Evidence of intermediates sometimes can be seen using techniques such as nuclear magnetic resonance spectroscopy
Explanation:
The study of reaction mechanism and chemical kinetics often form the main thrust of study in organic, inorganic and physical chemistry.
We often want to know the actual processes involved in the conversion of one specie to another. Unfortunately, this information may have to be obtained indirectly by certain chemical reactions or by the use of new instrumental methods such as nuclear magnetic resonance spectroscopy.
Many organic reactions have carbocation intermediates. These carbocations are relatively short-lived and are transient intermediates which are rarely isolated unless they are isolated in a molecular cage using a macromolecule or in superacids.
By intensive study, scientists can proof or disprove the authenticity of any proposed mechanism.
We must know that a transition state has partial bonds. It is often an extremely short-lived specie which cannot be isolated.
