answersLogoWhite

0

if cyclohexene is prepared by dehydration of cyclohexanol in the presence of a strong acide like H3PO4, sodium carbonate will be used to neutralize the acidic medium

User Avatar

Wiki User

11y ago

What else can I help you with?

Continue Learning about Natural Sciences

Why was cyclohexene with na2co3?

Cyclohexene reacts with sodium carbonate (Na2CO3) primarily as a mild base in various organic reactions, such as in the deprotonation of acidic protons or in nucleophilic substitution reactions. Sodium carbonate can help facilitate the formation of more reactive intermediates or stabilize anions during these processes. Additionally, it can act as a buffer to maintain a stable pH in the reaction environment, promoting optimal conditions for the desired chemical transformations.


Why receiving flask supposed to be kept on ice during preparation of cyclohexene?

Keeping the receiving flask on ice helps to condense the volatile cyclohexene vapors back into liquid form, making it easier to collect the product. This method ensures a higher yield of cyclohexene by preventing the loss of product due to vaporization.


What impurities present in cyclohexene before purification?

Before purification, cyclohexene may contain impurities such as water, which can result from the manufacturing process or handling, as well as residual solvents, unreacted starting materials, and by-products. Additionally, it may contain trace amounts of other hydrocarbons or aromatic compounds due to incomplete separation during synthesis. These impurities can affect the purity and reactivity of cyclohexene in subsequent applications.


What is Aragonite to Calcite?

•Aragonite is a metastable calcium carbonate • •Calcium carbonate is stable • •Will recrystallize to calcite during diagenesis


How many isomers does the dehydration of cyclohexanol have?

The dehydration of cyclohexanol can form two isomers: cyclohexene and cyclohexadiene. These isomers result from different locations of the double bond formed during the dehydration process.

Related Questions

Why was cyclohexene with na2co3?

Cyclohexene reacts with sodium carbonate (Na2CO3) primarily as a mild base in various organic reactions, such as in the deprotonation of acidic protons or in nucleophilic substitution reactions. Sodium carbonate can help facilitate the formation of more reactive intermediates or stabilize anions during these processes. Additionally, it can act as a buffer to maintain a stable pH in the reaction environment, promoting optimal conditions for the desired chemical transformations.


Why receiving flask supposed to be kept on ice during preparation of cyclohexene?

Keeping the receiving flask on ice helps to condense the volatile cyclohexene vapors back into liquid form, making it easier to collect the product. This method ensures a higher yield of cyclohexene by preventing the loss of product due to vaporization.


Why sodium carbonate is used in preparation of thiosulphate solution?

Sodium carbonate is used in the preparation of thiosulfate solution to help maintain a stable pH level during the reaction. It acts as a buffer to prevent large fluctuations in pH that could affect the reaction rate or yield of the thiosulfate solution. Additionally, sodium carbonate helps to dissolve the thiosulfate salt more effectively in water during the preparation process.


Why you add sodium carbonate to the mixture during preparation of ester?

Sodium carbonate is added during the preparation of esters to neutralize the acidic byproduct formed during the reaction. This helps to facilitate the esterification reaction and improve the yield of the desired ester product.


Why it is necessary to add sodium carbonate during the preparation of sodium fusion tube?

Sodium carbonate is added during the preparation of a sodium fusion tube to help create a more basic environment that promotes the formation of water-soluble compounds. This facilitates the extraction of certain metals or elements present in a sample through the formation of stable and soluble complexes. Additionally, sodium carbonate helps prevent the formation of unwanted side products during the fusion process.


Why the brown color of bromine disappear when mixed with cyclohexene?

Halogens react with alkenes to form haloalkanes. Addition of the bromine in this case occurs across the double bond in cyclohexene. The resultant products are colourless hence the brown colour disappears.


How cyclohexene might be formed as a byproduct in the synthesis of cyclohexanone?

Cyclohexene can be formed as a byproduct in the synthesis of cyclohexanone through dehydration of cyclohexanol. During the oxidation of cyclohexanol to cyclohexanone, some cyclohexanol may lose a water molecule, undergo dehydration, and form cyclohexene as a byproduct. This side reaction can occur when the temperature and reaction conditions favor dehydration over oxidation.


What impurities present in cyclohexene before purification?

Before purification, cyclohexene may contain impurities such as water, which can result from the manufacturing process or handling, as well as residual solvents, unreacted starting materials, and by-products. Additionally, it may contain trace amounts of other hydrocarbons or aromatic compounds due to incomplete separation during synthesis. These impurities can affect the purity and reactivity of cyclohexene in subsequent applications.


What was the salt like chemical that was used to embalm the organs?

Natron, the name of a naturally occurring sodium carbonate compound, was used in the embalming process during the preparation of mummies. Deposits of this mineral were mined from dry lake bottoms in Egypt.


What is Aragonite to Calcite?

•Aragonite is a metastable calcium carbonate • •Calcium carbonate is stable • •Will recrystallize to calcite during diagenesis


To avoid loss of nutrients during food preparation?

to avoid loss of nutrients food preparation


How many isomers does the dehydration of cyclohexanol have?

The dehydration of cyclohexanol can form two isomers: cyclohexene and cyclohexadiene. These isomers result from different locations of the double bond formed during the dehydration process.