Discuss the principle of estimation of halogens, sulphur and phosphorus present in an organic compound.
Estimation of halogens: It involves oxidising the organic substance with fuming nitric acid in the presence of silver nitrate. The halogen of the substance is thus converted to silver halide which is separated and weighed:
1Weight of organic compound = W gm
weight of silver halide = x g.
Estimation of sulphur: The organic substance is heated with fuming nitric acid but no silver nitrate is added. The sulphur of the substance is oxidised to sulphuric acid which is then precipitated as barium sulphate by adding excess of barium chloride solution. From the weight of BaSO4 so obtained the percentage of sulphur can be calculated.
Estimation of phosphorous: The organic substance is heated with fuming nitric acid whereupon phosphorous is oxidised to phosphoric acid. The phosphoric acid is precipitated as ammonium phosphomolybdate, (NH4)3 PO4 .12MOO3, by the addition of ammonia and ammonium molybdate solution which is then separated, dried and weighed.
Classify the following reactions in one of the reaction type studied in this unit.
(a) CH3CH2Br + HS– ———–> CH3CH2SH + Br–
(b) (CH3)2C=CH2 + HCl ———–> (CH3)2CCl—CH3
(c) CH3CH2Br + HO– ———–> CH2=CH2 + H2O + Br–
(d) (CH3)3C—CH2OH + HBr ———–> (CH3)2 C Br CH2CH2CH3 + H2O
In the Lassaigne’s test for ntrogen in an organic compound, the Prussian blue colour is obtaine d due to the formation of:
(a) Na4[Fe(CN)6] (b)Fe4[Fe(CN)6]3
(c) Fe2[Fe(CN)6] (d)Fe3[Fe(CN)6]4 .
Name a suitable technique of separation of the components from a mixture of calcium sulphate and camphor.
Why is it necessary to use acetic acid and not sulphric acid for acidification of sodium extract for testing sulphur by lead acetate test?
(a) 1 -Chloro-2-nitro-4-methylbenzene
(b) l-Chloro-4-methyl-2-nitrobenzene
(c) 2-Chloro-1 -nitro-5-methylbenzene
(d) m-Nitro-p-chlorotoluene
Electronegativity of carbon atoms depends upon their state of hybridization. In which of the following compounds, the carbon marked with asterisk is most electronegative?
In which of the following compounds the carbon marked with asterisk is expected to have greatest positive charge?
Which of the following represents the correct TUPAC name for the compounds concerned?
(a) 2, 2-Dimethylpentane or 2-Dimethylpentane (b) 2, 4, 7-Trimethyloctane or 2, 5, 7- Trimethyloctane (c) 2-Chloro-4-methylpentane or 4-Chloro-2-methylpentane (d) But-3-yn- l-ol or But-4-ol-yne.
What are electrophiles? Explain electrophile substitution reaction with the help of example.
Electrophilic addition reactions proceed in two steps. The first step involves the addition of an electrophile. Name the type of intermediate formed in the first step of the following addition reaction.
H3C-HC = CH2 + H+→ ?
(a) 2 °Carbanion
(b) 1 ° Carbocation
(c) 2 ° Carbocation
(d) l °Carbanion
Covalent bonds can undergo fission in two different ways. The correct representation involving the heterolytic fission of CH3 – Br is
Compounds with same molecular formula but differing in their structures are said to be structural isomers. What type of structural isomerism is shown by
Discuss the principle of estimation of halogens, sulphur and phosphorus present in an organic compound.
Hyperconjugation involves delocalization of .
(a) electrons of carbon-hydrogen σ bond of an alkyl group directly attached to an atom of unsatUrated system.
(b) electrons of carbon-hydrogen σ bond of alkyl group directly attached to the positively charged carbon atom.
(c) π-electrons of carbon-carbon bond.
(d) lone pair of electrons.
Describe the method, which can be used to separate two compounds with different solubilities in a solvent S.
Which of the following^ the correct IUPAC name?
(a) 3-Ethyl-4,4-dimethylheptane
(b) 4,4-Dimethyl-3-ethylheptane
(c) 5-Ethyl-4,4-dimethylheptane
(d) 4,4-Bis(methyl)-3-ethylheptane
Covalent bonds can undergo fission in two different ways. The correct representation involving the heterolytic fission of CH3 – Br is
What is the relationship between the members of following pairs of structures? Are they structural or geometrical isomers or resonance contributors?
Explain the reason for the fusion of an organic compound with metallic sodium for testing nitrogen, sulphur and halogens.
For testing halogens in an organic compound with AgN03 solution, sodium extract (Lassaigne's extract) is acidified with dilute HN03. What will happen if a student acidifies the extract with dilute H2S04 in place of dilute HN03?
Three students, Manish, Ramesh and Rajni, were determining the extra elements present in an organic compound given by their teacher. They prepared the Lassaigne's extract (LE) independently by the fusion of the compound with sodium metal. Then they added solid FeS04 and dilute sulphuric acid to a part of Lassaigne's extract. Manish and Rajni obtained Prussian blue colour bit Ramesh got red colour. Ramesh repeated the test with the same Lassaigne's extract, but again got red colour only. They were surprised and went to their teacher and told him about their observation. Teacher asked them to think over the reason for this. Can you help them by giving the reason for this observation? Also, write the chemical equations to explain the formation of compounds of different colours.
By mistake, an alcohol (boiling point 97 °C) was mixed with a hydrocarbon (boiling point 68 °C). Suggest a suitable method to separate the two compounds. Explain the reason for your choice.
What are hybridisation states of each carbon atom in the following compounds? CH2=C=O, CH3CH=CH2, (CH3)2CO, CH2=CHCN, C6H6.
(a) What do you understand by Homolytic fission?
(b) What are carbanions? Give an example.
0.15 g of an organic compound gave 0.12 g of Ag Br by the Carius method. Find percentage of Br in the compound.
In which of the following representations given below spatial arrangement of group/atom is different from that given in structure ‘A'?
Will CCl4 give white precipitate of AgCl on heating it with silver nitrate? Give reason for your answer.
Give equation for the following:
(i) Electrophilic Substitution
(ii) Nucleophilic Substitution
(a) 2-Ethyl-3-methylpentane
(b) 3,4-Dimethylhexane
(c) 2-sec-Butylbutane
(d) 2,3-Dimethylbutane
The IUPAC name for
(a) 1-Hydroxypentane-l, 4-dione
(b) 1,4-Dioxopentanol
(c) l-Carboxybutan-3-one
(d) 4-Oxopentanoic acid
