How do you convert fractions to what?
to convert means to change
18cm convert into mm
That depends what you want to convert it to.That depends what you want to convert it to.That depends what you want to convert it to.That depends what you want to convert it to.
To convert inches to centimeters, multiply by 2.54. To convert from centimeters to inches, divide by the same factor.To convert inches to centimeters, multiply by 2.54. To convert from centimeters to inches, divide by the same factor.To convert inches to centimeters, multiply by 2.54. To convert from centimeters to inches, divide by the same factor.To convert inches to centimeters, multiply by 2.54. To convert from centimeters to inches, divide by the same factor.
The potassium hydroxide (KOH) expression for aniline (C6H5NH2) is C6H5NH2 + KOH → C6H5NH2K + H2O.
The KB expression for aniline c6h5nh2 is: For C6H5NH2 + H2O >< C6H5NH3+ + OH-Kb = 4.3 x (10 ^ -10) = [C6H5NH3+][OH-] / [C6H5NH2]
The condensed structural formula of aniline is C6H5NH2.
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+).
The cation would be C6H5NH3+ and the anion would be C6H5NH-
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
The chemical fomula of aniline is C6H7N.
'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)
The balanced equation for the reaction of C6H5MgBr with ammonia (NH3) is: C6H5MgBr + 2NH3 -> C6H5NH2 + Mg(OH)Br
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).
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.
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.