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How will you convert ethyl bromide into butane?
Ethyl bromide can be converted into butane through a series of steps involving elimination reactions. The ethyl bromide can be treated with a strong base, such as sodium ethoxide, to form ethylene gas. Ethylene gas can then be subjected to a hydrogenation reaction to produce butane.
What is the equation for the reaction of ethyl-4-aminobenzoate and sodium hydroxide?
The reaction between ethyl-4-aminobenzoate and sodium hydroxide will result in the formation of sodium 4-aminobenzoate and ethanol through a nucleophilic substitution reaction in which the ethyl group is replaced by the sodium ion. The balanced chemical equation for this reaction is: Ethyl-4-aminobenzoate + Sodium hydroxide → Sodium 4-aminobenzoate + Ethanol
What is the hydrolysis product of ethyl propanoate and aqueous sodium hydroxide?
The hydrolysis of ethyl propanoate with aqueous sodium hydroxide will produce propanoic acid and ethyl alcohol.
Equation for the ethyl acetate test?
The ethyl acetate test is a qualitative test used to detect the presence of acetoacetic acid in urine. The equation involves the reaction of acetoacetic acid in urine with ethyl acetate in the presence of a mineral acid like hydrochloric acid. The equation can be represented as: CH3COCH2COOH (acetoacetic acid) + CH3COOCH2CH3 (ethyl acetate) + HCl → no visible change A positive result is indicated by the production of a pink or red color in the upper ethyl acetate layer due to the formation of sodium nitroprusside complex with acetoacetic acid.
Why is sodium chloride insoluble in ethyl alcohol?
Sodium chloride is insoluble in ethyl alcohol because the bonding between sodium and chloride ions in sodium chloride is very strong due to ionic attractions. Ethyl alcohol is a non-polar solvent, which cannot break these strong ionic bonds to dissolve sodium chloride.
How will you convert ethyl bromide into butane?
Ethyl bromide can be converted into butane through a series of steps involving elimination reactions. The ethyl bromide can be treated with a strong base, such as sodium ethoxide, to form ethylene gas. Ethylene gas can then be subjected to a hydrogenation reaction to produce butane.
What is the equation for the reaction of ethyl-4-aminobenzoate and sodium hydroxide?
The reaction between ethyl-4-aminobenzoate and sodium hydroxide will result in the formation of sodium 4-aminobenzoate and ethanol through a nucleophilic substitution reaction in which the ethyl group is replaced by the sodium ion. The balanced chemical equation for this reaction is: Ethyl-4-aminobenzoate + Sodium hydroxide → Sodium 4-aminobenzoate + Ethanol
What represents c6h14?
A saturated hydrocarbon (alkane). This can mean hexane, methyl pentane, ethyl butane, dimethyl butane etc.
What is the hydrolysis product of ethyl propanoate and aqueous sodium hydroxide?
The hydrolysis of ethyl propanoate with aqueous sodium hydroxide will produce propanoic acid and ethyl alcohol.
Is sodium chloride soluble in ethyl acetate?
No, sodium chloride is not soluble in ethyl acetate. Ethyl acetate is a nonpolar solvent, while sodium chloride is an ionic compound that is highly soluble in water but not in nonpolar solvents like ethyl acetate.
Equation for the ethyl acetate test?
The ethyl acetate test is a qualitative test used to detect the presence of acetoacetic acid in urine. The equation involves the reaction of acetoacetic acid in urine with ethyl acetate in the presence of a mineral acid like hydrochloric acid. The equation can be represented as: CH3COCH2COOH (acetoacetic acid) + CH3COOCH2CH3 (ethyl acetate) + HCl → no visible change A positive result is indicated by the production of a pink or red color in the upper ethyl acetate layer due to the formation of sodium nitroprusside complex with acetoacetic acid.
Why is sodium chloride insoluble in ethyl alcohol?
Sodium chloride is insoluble in ethyl alcohol because the bonding between sodium and chloride ions in sodium chloride is very strong due to ionic attractions. Ethyl alcohol is a non-polar solvent, which cannot break these strong ionic bonds to dissolve sodium chloride.
What is the equation for producing ethyl propanoate from iodoethane?
To produce ethyl propanoate from iodoethane, you would first need to react iodoethane (CH3CH2I) with sodium propanoate (CH3CH2COONa) in the presence of dry ethanol (CH3CH2OH) or other esterification catalysts. The reaction would result in the formation of ethyl propanoate (CH3CH2COOCH2CH3) along with sodium iodide (NaI) as a byproduct.
Which has a higher melting point Sodium Chloride or Ethyl Alcohol?
Sodium Chloride has a higher melting point because at room temperature it is a solid but Ethyl alcohol has already melted, as it is liquid.
Why is sodium sulfate insoluble in ethyl alcohol?
Sodium sulfate is a polar compound, ethanol is not polar.
What hydrocarbon is obtained when Na metal react with ethyl bromide in presence of anhydrous ether?
By Wurtz reaction Butane is formed.
How do you draw the structure 5-chloro-3-ethyl-4-methyloctane?
To begin with, octane is a chain of 8 carbons. If you were to draw these eight carbons in a row and number them 1-8, then the numbers corresponding to the substituents (chloro, ethyl and methyl) will show you where to put them. Off of the fifth carbon from one end (make sure you are consistent with which end you use!) is Cl Off of the third carbon is the ethyl group (CH2-CH3) and off of the fourth is the methyl group (CH3)
