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Tuesday, 9 August 2016
organic chemistry tutor in JANAKPURI-9958510549
organic chemistry tutor in JANAKPURI-9958510549
Contact 9716957220
Organic chemistry [Distinguish test]
Acetophenone and Benzaldehayde.
Prpanone and propanol.
Propanal and propanone
Phenol and Benzoic acid
Ethanal and propanal
Ethylamine and Aniline
Methylamine [1o amine] and Dimethylamine[2o amine]
Benzoic acid and ethyl benzoate
Aniline and Benzylamine
Aniline and N-methylaniline
Benzaldehyde and Acetophenone
Acetophenone and Benzophenone
Primary alcohol and secondry alcohol.
Phenol and Alcohol
Methyl ethanoate and ethyl ethanoate
Secondry amine and tertiary amine
Methanol and ethanol
Chlorobenzene and benzylchloride
Ethanol and Diethyl ether
Ethyl amine and Ethane amide.
Chloroform and carbon tetra chloride.
Organic chemistry [important name reaction]
Cannizaro reaction [m. imp]
Cross aldol condensation
Decarboxylation
Hoffman’s bromamide reaction
Gabrial phathalimide
Acetylation
Reimmer tiemmer reaction
Williamson’s synthesis
Gatterman
Coupling
Clemmension reduction
H.V.Z. reaction
Kolbe’s reaction
Wolf kishner reduction
Carbylamine reaction
Ammonolysis
Friedal craft reaction
Sandmeyer’s reaction
Wurtz reaction
Hinsberg’s test foer amines
Aldol condensation
Organic chemistry [Reasoning]
Pka value of carboxylic acid is decreases on increases electronegative group with carboxylic acid.
Haloarenes are much less reactive than haloalkanes towards Nucleophilic substitution reaction.
Why 1> 2> 3o faster in Sn2? And 3> 2> 1o faster in Sn1?
Pkb for aniline is more than that for methylamine
Methylamine react with ferric chloride to give precitate of ferric hydroxide.
Aniline does not undergo friedal craft reaction
Aldehydes are more reactive than ketones towards nucleophiles
Boiling point of aldehydes and ketones are lower than of the corresponding acids as well as alcohols
Aldehydes and ketones undergo a no. addition reaction
Ethanoic acid is weaker acid than benzoic acid
Basic strength arrangement of amines[m. imp]
Why phenol do not give protation reaction readily
Boiling point of ethanol is higher than methoxymethane
Phenol is more acidic than alcohol [ethanol]
O-P – nitrophenol are more acidic than phenol
Why primary amines have higher boiling than tertiary amines.amines
Dipole moment of chlorobenzene is lower than that of cyclohexyl chloride
Alkyl halides though polar but immisible with water
What is racemic mixture
Chloromethane reacts with KCN to form ethane nitrile as main product but with AgCN to form methyl isocynide
Benzyl halides show high reactivity towards Sn1.
Benzoic acid does not undergo friedal craft reaction.
Gabriel phathalimide reaction give only primary amines and it also do not give aniline?
Why Aniline give nitration on substantial amount on m –position?
Why aniline do not give direct nitration?
What is the limitations of Williamsons synthesis reagent?
What happens when excess of HI is reacted with ether
Why 2,2,5 trimethylcyclohexanone do not give cynohydrin very easily?
Why during formation of ester water shoid be removed imiediately?
Why carboxylic acid is acidic than phenol?
Organic chemistry [conversions and mechanism]
Benzene diazonium chloride --( Nitro benzene
Aniline -( Benzene diazonium chloride
Ethylamine --( methyl amine
Ethyl benzene ---( Benzoic acid
Toluene ----( Benzaldehyde [Etard reaction]
Propanone ----( propene
Benzoic acid ----( Benzaldehyde
Bromo benzene ---( 1-phenyl ethanol
Dehydration of alcohol [mechanisms]
Hydration of ethane ---( ethanol [mechanism]
Chloroethane ---( propan-1-amine
Ethane amine --( N-ethylethane amide
Primary alcohol ---( Aldehyde
Butan-2-one ---( Butan-2-ol
Phenol ----( 2,4,6-tri bromo phenol
Name the Organic compound 69.77% carbon 11.63% hydrogen and rest is oxygen. Molecular mass is 86.
Benzene -----( Acetophenone
Ethanol -----( 3- hydroxyl butane
Benzaldehyde----( Benzophenone
Organic compound A (C8 H16 O2). Its gets hydrolysed with dilute sulphuric acid and give B (carboxylic acid) and alcohol(C). oxidation of ‘C’ with chromic acid also produced B. C on dehydration gives but-1-ene. Write equations for the reactions involved.
Benzyl chloride ------( Benzyl alcohol
Methyl magnesium bromide -----( 2-methyl propan-2-ol
Ethanol ------( But-2-enal
Propanone------( 2-methyl propan-2-ol
Bromo benzene -------( Benzoic acid
Ethyl cyanide------( Etanoic acid
Methyl Benzene-----( Benzoic acid
A + Cl2-----(CHCl3 + NaOH ---(B + C6H5COCl---( C + C6H6/Alcl3----(D + E.
Phenol ----( Picric acid
Toluene + CrO3 + acetic anhydride (273-283K) ---( A + H2O/H+ --(B + conc. NaOH ---( C + sodiumbenzoate
Toluene + KmnO4 +KOH ----( A + H2O/H+ -----( E.
Organic chemistry [Distinguish test]
Acetophenone and Benzaldehayde.
Prpanone and propanol.
Propanal and propanone
Phenol and Benzoic acid
Ethanal and propanal
Ethylamine and Aniline
Methylamine [1o amine] and Dimethylamine[2o amine]
Benzoic acid and ethyl benzoate
Aniline and Benzylamine
Aniline and N-methylaniline
Benzaldehyde and Acetophenone
Acetophenone and Benzophenone
Primary alcohol and secondry alcohol.
Phenol and Alcohol
Methyl ethanoate and ethyl ethanoate
Secondry amine and tertiary amine
Methanol and ethanol
Chlorobenzene and benzylchloride
Ethanol and Diethyl ether
Ethyl amine and Ethane amide.
Chloroform and carbon tetra chloride.
Organic chemistry [important name reaction]
Cannizaro reaction [m. imp]
Cross aldol condensation
Decarboxylation
Hoffman’s bromamide reaction
Gabrial phathalimide
Acetylation
Reimmer tiemmer reaction
Williamson’s synthesis
Gatterman
Coupling
Clemmension reduction
H.V.Z. reaction
Kolbe’s reaction
Wolf kishner reduction
Carbylamine reaction
Ammonolysis
Friedal craft reaction
Sandmeyer’s reaction
Wurtz reaction
Hinsberg’s test foer amines
Aldol condensation
Organic chemistry [Reasoning]
Pka value of carboxylic acid is decreases on increases electronegative group with carboxylic acid.
Haloarenes are much less reactive than haloalkanes towards Nucleophilic substitution reaction.
Why 1> 2> 3o faster in Sn2? And 3> 2> 1o faster in Sn1?
Pkb for aniline is more than that for methylamine
Methylamine react with ferric chloride to give precitate of ferric hydroxide.
Aniline does not undergo friedal craft reaction
Aldehydes are more reactive than ketones towards nucleophiles
Boiling point of aldehydes and ketones are lower than of the corresponding acids as well as alcohols
Aldehydes and ketones undergo a no. addition reaction
Ethanoic acid is weaker acid than benzoic acid
Basic strength arrangement of amines[m. imp]
Why phenol do not give protation reaction readily
Boiling point of ethanol is higher than methoxymethane
Phenol is more acidic than alcohol [ethanol]
O-P – nitrophenol are more acidic than phenol
Why primary amines have higher boiling than tertiary amines.amines
Dipole moment of chlorobenzene is lower than that of cyclohexyl chloride
Alkyl halides though polar but immisible with water
What is racemic mixture
Chloromethane reacts with KCN to form ethane nitrile as main product but with AgCN to form methyl isocynide
Benzyl halides show high reactivity towards Sn1.
Benzoic acid does not undergo friedal craft reaction.
Gabriel phathalimide reaction give only primary amines and it also do not give aniline?
Why Aniline give nitration on substantial amount on m –position?
Why aniline do not give direct nitration?
What is the limitations of Williamsons synthesis reagent?
What happens when excess of HI is reacted with ether
Why 2,2,5 trimethylcyclohexanone do not give cynohydrin very easily?
Why during formation of ester water shoid be removed imiediately?
Why carboxylic acid is acidic than phenol?
Organic chemistry [conversions and mechanism]
Benzene diazonium chloride --( Nitro benzene
Aniline -( Benzene diazonium chloride
Ethylamine --( methyl amine
Ethyl benzene ---( Benzoic acid
Toluene ----( Benzaldehyde [Etard reaction]
Propanone ----( propene
Benzoic acid ----( Benzaldehyde
Bromo benzene ---( 1-phenyl ethanol
Dehydration of alcohol [mechanisms]
Hydration of ethane ---( ethanol [mechanism]
Chloroethane ---( propan-1-amine
Ethane amine --( N-ethylethane amide
Primary alcohol ---( Aldehyde
Butan-2-one ---( Butan-2-ol
Phenol ----( 2,4,6-tri bromo phenol
Name the Organic compound 69.77% carbon 11.63% hydrogen and rest is oxygen. Molecular mass is 86.
Benzene -----( Acetophenone
Ethanol -----( 3- hydroxyl butane
Benzaldehyde----( Benzophenone
Organic compound A (C8 H16 O2). Its gets hydrolysed with dilute sulphuric acid and give B (carboxylic acid) and alcohol(C). oxidation of ‘C’ with chromic acid also produced B. C on dehydration gives but-1-ene. Write equations for the reactions involved.
Benzyl chloride ------( Benzyl alcohol
Methyl magnesium bromide -----( 2-methyl propan-2-ol
Ethanol ------( But-2-enal
Propanone------( 2-methyl propan-2-ol
Bromo benzene -------( Benzoic acid
Ethyl cyanide------( Etanoic acid
Methyl Benzene-----( Benzoic acid
A + Cl2-----(CHCl3 + NaOH ---(B + C6H5COCl---( C + C6H6/Alcl3----(D + E.
Phenol ----( Picric acid
Toluene + CrO3 + acetic anhydride (273-283K) ---( A + H2O/H+ --(B + conc. NaOH ---( C + sodiumbenzoate
Toluene + KmnO4 +KOH ----( A + H2O/H+ -----( E.
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