Propanal (CH3CH2CHO) can be converted to Propane (CH3CH2CH3) by Clemmensen reduction using Zn-Hg and conc. HCl or Wolff-Kishner reduction using NH2NH2 followed by KOH in ethylene glycol.
Ethanal (CH3CHO) undergoes Aldol condensation in the presence of dilute NaOH to form 3-hydroxybutanal, which upon heating loses a water molecule to form But-2-enal (CH3CH=CHCHO).
Ethanoic acid (CH3COOH) reacts with ammonia (NH3) to form ammonium ethanoate (CH3COONH4), which upon strong heating undergoes dehydration to form Ethanamide (CH3CONH2).
The rate of a reaction is defined as the change in concentration of any one of the reactants or products per unit time. Mathematically, for a general reaction aA + bB -> cC + dD, it is expressed as: Rate = -(1/a)(d[A]/dt) = -(1/b)(d[B]/dt) = (1/c)(d[C]/dt) = (1/d)(d[D]/dt).
The rate of disappearance of H2(g) is defined as the negative rate of change of its molar concentration over time: Rate of disappearance of H2 = -d[H2]/dt.
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Log in to view solution →Amines constitute an important class of organic compounds derived by replacing one or more hydrogen atoms of ammonia molecule by alkyl/aryl groups. Amines are usually formed from nitro compounds, halides, amides, etc. They exhibit hydrogen bonding which influences their physical properties. Alkyl amines are found to be stronger bases than ammonia. In aromatic amines, electron releasing and withdrawing groups, respectively increase and decrease their basic character. Reactions of amines are governed by availability of the unshared pair of electrons on nitrogen. Influence of the number of hydrogen atoms at nitrogen atom on the type of reactions and nature of products is responsible for identification and distinction between primary, secondary and tertiary amines. Reactivity of aromatic amines can be controlled by acylation process.
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