Chemistry
Give equations for the conversions of – Methane, Ethane:
Methane to | Ethane to | |
---|---|---|
(a) Carbon tetrachloride | (a) Hexachloro ethane | by - Substitution [diffused sunlight] |
(b) Carbon dioxide | (b) Carbon dioxide | by - Oxidation - Complete |
(c) Methanol to Methanal to Methanoic acid | Ethanol to Ethanal to Ethanoic acid | by - Oxidation (i) catalytic using - catalyst copper [Cu] (ii) Controlled using acidified K2Cr2O7 |
(d) Methnal | Ethanal | by- Oxidation - Catalytic - using catalyst MoO |
(e) Ethyne | Ethene | by - Pyrolysis [dehydrogenation] |
Organic Chemistry
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Answer
(a) Conversion of Methane to Carbon tetrachloride by substitution [diffused sunlight]:
4} + 4\text{Cl}2 \xrightarrow[\Delta]{\text{diffused sunlight}} \underset{\text{Carbon tetrachloride}}{\text{CCl}_4} + 4\text{HCl}
(b) Conversion of Methane to Carbon dioxide by complete oxidation:
4} + 2\text{O}2\text{[excess]} \longrightarrow \text{CO}2 + 2\text{H}2\text{O} + \Delta
(c)(i) Conversion of Methane to Methanol to Methanal to Methanoic acid by catalytic oxidation using catalyst copper [Cu]:
4} + \text{O}2 \xrightarrow[200 \text{\degree C}]{\text{Cu tube}} \underset{\text{methanol}}{2\text{CH}3\text{OH}} \\[1em] \underset{\text{methanol}}{2\text{CH}3\text{OH}} + \text{O}2 \xrightarrow[\text{catalyst}]{\text{Cu}} \underset{\text{methanal} }{\text{2HCHO}} + 2\text{H}2\text{O} \\[1em] \underset{\text{methanal} }{\text{2HCHO}} + \text{O}_2 \xrightarrow[\text{catalyst}]{\text{Cu}} \underset{\text{methanoic acid} }{\text{2H-COOH}}
(c)(ii) Conversion of Methane to Methanol to Methanal to Methanoic acid by controlled slow oxidation using acidified K2Cr2O7:
4} \xrightarrow[\text{K}2\text{Cr}2\text{O}7]{\text{[O]}} \underset{\text{ methanol}}{\text{CH}3\text{OH}} \xrightarrow[\text{K}2\text{Cr}2\text{O}7]{\text{[O]}} \underset{\text { methanal}}{\text{HCHO}} \xrightarrow[\text{K}2\text{Cr}2\text{O}_7]{\text{[O]}} \underset{\text{methanoic acid} }{\text{HCOOH}}
(d) Conversion of Methane to Methanal by catalytic oxidation using catalyst MoO:
4} + \text{O}2 \xrightarrow[350 - 500 \text{\degree C}]{\text{MoO}} \underset{\text{methanal} }{\text{HCHO}} + \text{H}_2\text{O}
(e) Conversion of Methane to Ethyne by Pyrolysis [dehydrogenation]:
4} \xrightarrow{1500 \degree \text{C}} \underset{\text{ethyne} }{\text{C}2\text{H}2} + 3\text{H}2
(a) Conversion of Ethane to Hexachloro ethane by substitution [diffused sunlight]:
2\text{H}6} + \text{Cl}2 \underset{\Delta}{\xrightarrow{\text{diffused sunlight}}} \underset{\text{monochloroethane}}{\text{C}2\text{H}_5\text{Cl}}+ \text{HCl}
2\text{H}5\text{Cl}} + \underset{\text{[excess]}}{\text{Cl}2} \longrightarrow \underset{\text{dichloroethane}}{\text{C}2\text{H}4\text{Cl}2}+ \text{HCl}
2\text{H}4\text{Cl}2} + \text{Cl}2 \longrightarrow \underset{\text{trichloroethane}}{\text{C}2\text{H}3\text{Cl}_3}+ \text{HCl}
2\text{H}3\text{Cl}3} + \text{Cl}2 \longrightarrow \underset{\text{tetrachloroethane}}{\text{C}2\text{H}2\text{Cl}_4}+ \text{HCl}
2\text{H}2\text{Cl}4} + \text{Cl}2 \longrightarrow \underset{\text{pentachloroethane}}{\text{C}2\text{H}\text{Cl}5}+ \text{HCl}
2\text{H}\text{Cl}5} + \text{Cl}2 \longrightarrow \underset{\text{hexachloroethane}}{\text{C}2\text{Cl}_6}+ \text{HCl}
(b) Conversion of Ethane to Carbon dioxide by complete oxidation:
2\text{H}6} + 7\text{O}2\text{[excess]} \longrightarrow \text{4CO}2 + 6\text{H}_2\text{O} + \Delta
(c)(i) Conversion of Ethane to Ethanol to Ethanal to Ethanoic acid by catalytic oxidation using catalyst copper [Cu]:
2\text{H}6} + \text{O}2 \xrightarrow[200 \text{\degree C}]{\text{Cu tube}} \underset{\text{ethanol}}{2\text{C}2\text{H}5\text{OH}} \\[1em] \underset{\text{ethanol}}{2\text{C}2\text{H}5\text{OH}} + \text{O}2 \xrightarrow[\text{catalyst}]{\text{Cu}} \underset{\text{ethanal}}{2\text{CH}3\text{CHO}} + 2\text{H}2\text{O} \\[1em] \underset{\text{ethanal}}{2\text{CH}3\text{CHO}} + \text{O}2 \xrightarrow[\text{catalyst}]{\text{Cu}} \underset{ \text{ethanoic acid} }{2\text{CH}_3\text{COOH}}
(c)(ii) Conversion of Ethane to Ethanol to Ethanal to Ethanoic acid by controlled slow oxidation using acidified K2Cr2O7:
2\text{H}6} \xrightarrow[\text{K}2\text{Cr}2\text{O}7]{\text{[O]}} \underset{ \text{ethanol}}{\text{C}2\text{H}5\text{OH}} \xrightarrow[\text{K}2\text{Cr}2\text{O}7]{\text{[O]}} \underset{\text{ethanal}}{\text{CH}3\text{CHO}} \xrightarrow[\text{K}2\text{Cr}2\text{O}7]{\text{[O]}} \underset{\text{ethanoic acid}}{\text{CH}_3\text{COOH}}
(d) Conversion of Ethane to Ethanal by catalytic oxidation using catalyst MoO:
2\text{H}6} + \text{O}2 \xrightarrow[350 - 500 \text{\degree C}]{\text{MoO}} \underset{\text{ethanal} }{\text{CH}3\text{CHO}} + \text{H}_2\text{O}
(e) Conversion of Ethane to Ethene by Pyrolysis [dehydrogenation]:
2\text{H}6} \xrightarrow[\text{catalyst [Al}2\text{O}3\text{]}]{500 \degree \text{C}} \underset{\text{ethene}}{\text{C}2\text{H}4} + \text{H}_2
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Related Questions
Give the IUPAC name of the compounds numbered (i) to (v).
Give balanced equations for the laboratory preparations of - Alkanes, Alkenes, Alkynes, Alcohols and Acids.
Sl.
No.Compound from: by/from: (a) Methane [CH4] Sodium ethanoate [sodium acetate] by -decarboxylation (b) Methane [CH4] Iodo methane [methyl iodide] from -an alkylhalide (c) Ethane [C2H6] Sodium propanoate [sodium propionate] by -decarboxylation (d) Ethane [C2H6] Bromo ethane [ethyl bromide] from -alkylhalide (e) Ethene [C2H4] from ethanol [ethyl alcohol] by -dehydration (f) Ethene [C2H4] Bromo ethane [ethyl bromide] by - dehydrohalogenation (g) Ethyne [C2H2] from calcium carbide from -a calcium compound (h) Ethyne [C2H2] 1,2, dibromoethane [ethylene dibromide] by -dehydrohalogenation (i) Ethanol [C2H5OH] Bromo ethane [ethyl bromide] by - hydrolysis of alkylhalide (j) Ethanol [C2H5OH] Ethene [ethylene] by - hydration of ethene (k) Ethanoic acid [CH3COOH] Ethanol [ethyl alcohol] by - oxidation of alcohol Give equations for the conversions of – Ethene, Ethyne to:
Ethene Ethyne (a) Ethane (a) Ethane [2 steps ] by - Catalytic hydrogenation - H2 (b) 1,2 dichloroethane (b) 1,1,2,2 tetrachloroethane [2 steps] by- Halogenation - Cl2 (c) 1,2 dibromoethane (c) 1,1,2,2 tetrabromoethane [2 steps] - Br2 (d) 1,2 diiodoethane (d) 1,2 diiodoethene - I2 (e) Bromoethane/Chloroethane (e) 1,1 -dibromo & 1,1-dichloroethane by- Halogen acids - HBr/HCl
by - Polymerization(f) Polyethylene (f) Copper or silver Acetylide by Ammoniacal - CuCl/AgNO3 Give equations for the conversions of – Ethanol and Ethanoic Acid to:
Ethanol [ethyl alcohol] Ethanoic Acid [acetic acid] (a) Carbon dioxide - by burning (a) Sodium acetate - using alkali - NaOH (b) Ethanal
to
Ethanoic acid - by oxidation using acidified K2Cr2O7(b) Calcium acetate - using alkali - Ca(OH)2 (c) Sodium ethaoxide - using - sodium (c) Ammonium acetate - using alkali - NH4OH (d) Ethyl ethanoate - using - ethanoic acid and conc. H2SO4 (d) Ethyl ethanoate -using - ethanol and conc. H2SO4 [ethyl acetate] (e) Ethene - using conc. H2SO4 at 170 °C