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Q: How do you convert c6h5nh2 to c6h5ococh3?
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What is the KB expression for aniline c6h5nh2?

The potassium hydroxide (KOH) expression for aniline (C6H5NH2) is C6H5NH2 + KOH → C6H5NH2K + H2O.


What is the KB expression for aniline?

The KB expression for aniline c6h5nh2 is: For C6H5NH2 + H2O >< C6H5NH3+ + OH-Kb = 4.3 x (10 ^ -10) = [C6H5NH3+][OH-] / [C6H5NH2]


What is the condensed structural formula of Aniline?

The condensed structural formula of aniline is C6H5NH2.


What is the dissociation reaction for anilinium ion?

The dissociation reaction of anilinium ion (C6H5NH3+) in water is: C6H5NH3+ (aq) -> C6H5NH2 (aq) + H+ (aq). In this reaction, anilinium ion breaks apart into aniline (C6H5NH2) and a hydrogen ion (H+).


What are the cation and anion for aniline (C6H5NH2)?

The cation would be C6H5NH3+ and the anion would be C6H5NH-


What is the balance equation for the reaction of aniline with HCL?

Anthracene is a hydrocarbon with chemical formula C14H10. When it undergoes complete combustion it forms water vapour and carbon dioxide. 2 C14H10 + 33 O2 → 10 H2O + 28 CO2


What is formula of aniline?

The chemical fomula of aniline is C6H7N.


What is the conjugate base of C6H5COOH?

'Conjugate' means ONE proton (H+) more (acid) or less (base) than the described acid or base respectively:So the conjugate acid of C6H5NH2 is C6H5NH3+ (phenylammonium cation)


What is the Balanced equation for the reaction of c6h5mgbr with ammonia?

The balanced equation for the reaction of C6H5MgBr with ammonia (NH3) is: C6H5MgBr + 2NH3 -> C6H5NH2 + Mg(OH)Br


Why aniline is weaker base than methylamine?

Since tha pka of the aniline ion is equal to 4.6, the anilinium ion is a stronger acid than the methylaminium ion, and aniline (c6h5nh2) is a weaker base than methylamine (ch3nh2).


What are example of weak base?

Examples of weak bases include ammonia (NH3), methylamine (CH3NH2), and aniline (C6H5NH2). These compounds do not completely dissociate in water to release hydroxide ions but can still react with acids to form salts and water.


How do you Prepare sulphanilic acid from phenyl amine?

Sulphanilic acid can be prepared from aniline by diazotization with sodium nitrite in acidic conditions to form diazonium salt, followed by heating or treatment with sulfur dioxide gas to convert the diazonium salt to sulphanilic acid.