The Reaction Of Ethanol With Conc. H2SO4gives - Vedantu

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seo-qnaheader left imagearrow-right Answerdown arrowQuestion Answers for Class 12down arrowClass 12 BiologyClass 12 ChemistryClass 12 EnglishClass 12 MathsClass 12 PhysicsClass 12 Social ScienceClass 12 Business StudiesClass 12 EconomicsQuestion Answers for Class 11down arrowClass 11 EconomicsClass 11 Computer ScienceClass 11 BiologyClass 11 ChemistryClass 11 EnglishClass 11 MathsClass 11 PhysicsClass 11 Social ScienceClass 11 AccountancyClass 11 Business StudiesQuestion Answers for Class 10down arrowClass 10 ScienceClass 10 EnglishClass 10 MathsClass 10 Social ScienceClass 10 General KnowledgeQuestion Answers for Class 9down arrowClass 9 General KnowledgeClass 9 ScienceClass 9 EnglishClass 9 MathsClass 9 Social ScienceQuestion Answers for Class 8down arrowClass 8 ScienceClass 8 EnglishClass 8 MathsClass 8 Social ScienceQuestion Answers for Class 7down arrowClass 7 ScienceClass 7 EnglishClass 7 MathsClass 7 Social ScienceQuestion Answers for Class 6down arrowClass 6 ScienceClass 6 EnglishClass 6 MathsClass 6 Social ScienceQuestion Answers for Class 5down arrowClass 5 ScienceClass 5 EnglishClass 5 MathsClass 5 Social ScienceQuestion Answers for Class 4down arrowClass 4 ScienceClass 4 EnglishClass 4 MathsSearchIconbannerThe reaction of ethanol with conc. ${{\text{H}}_{2}}\text{S}{{\text{O}}_{4}}$gives: A. ethaneB. etheneC. ethyneD. ethanoic acid AnswerVerifiedVerified575.7k+ viewsHint: The reaction between ethanol and conc. ${{\text{H}}_{2}}\text{S}{{\text{O}}_{4}}$ is a dehydration reaction. Dehydration means removal of water molecules to form alkenes. As concentrated ${{\text{H}}_{2}}\text{S}{{\text{O}}_{4}}$ is a dehydrating agent. Ethanol has two carbon atoms and an alcohol group and rest vacancies are filled by hydrogen atoms. Complete answer: Let us form the product of this reaction using the mechanism:Step (1)- Attack of ${{\text{H}}^{+}}$ ion on the lone pair of oxygen atom, as the ${{\text{H}}^{+}}$ ion is electron deficient and lone pairs are electron rich. The ${{\text{H}}^{+}}$ ion is formed from dissociation of sulphuric acid into its respective ions $\left( \text{2}{{\text{H}}^{+}}+\text{SO}_{4}^{2-} \right)$. This attack on lone pairs leads to formation of protonated alcohol. seo images Step (2)- Removal of water occurs from the protonated alcohol to form carbocation. This is a slow step or rate-determining step. The rate of any reaction is determined by the slowest step. seo images Step (3)- Formation of alkene or ethene takes place by the elimination of ${{\text{H}}^{+}}$ion from the carbocation. The ${{\text{H}}^{+}}$ion is a catalyst of this reaction as it remains unutilized. seo images The correct answer to this question is ethene is formed as a product on reaction between ethanol and conc. ${{\text{H}}_{2}}\text{S}{{\text{O}}_{4}}$ So, the correct answer is “Option B”.Additional Information:Secondary and tertiary alcohols dehydrate under mild conditions only because after protonation, the carbocation formed is highly stable due to hyperconjugation. Thus, the relative ease of dehydration of alcohols is $\text{Tertiary}>\text{Secondary}>\text{Primary}$. Note: Alcohols reacts with conc.${{\text{H}}_{2}}\text{S}{{\text{O}}_{4}}$ not only to form alkenes but at different temperatures, the reactions are different thus, the products formed are different. Like, (1) At 383 K, ethanol reacts with sulphuric acid to form ethyl hydrogen sulphate and water. ${{\text{C}}_{2}}{{\text{H}}_{5}}\text{OH}+\text{conc}\text{.}{{\text{H}}_{2}}\text{S}{{\text{O}}_{4}}\xrightarrow{383\text{K}}{{\text{C}}_{2}}{{\text{H}}_{5}}\text{HS}{{\text{O}}_{4}}+{{\text{H}}_{2}}\text{O}$ (2) At 413 K, ethanol reacts with sulphuric acid to form diethyl ether. As, the two molecules of ethanol combine to remove water. ${{\text{C}}_{2}}{{\text{H}}_{5}}\text{OH}+\text{conc}\text{.}{{\text{H}}_{2}}\text{S}{{\text{O}}_{4}}\xrightarrow{413\text{K}}{{\text{C}}_{2}}{{\text{H}}_{5}}{\mathrm O}{{\text{C}}_{2}}{{\text{H}}_{5}}+{{\eta }_{2}}{\mathrm O}$ (3) At 443 K, ethanol reacts with sulphuric acid to form ethene. Ethanol gets protonated and water gets removed. ${{\text{C}}_{2}}{{\text{H}}_{5}}\text{OH}+\text{conc}\text{.}{{\text{H}}_{2}}\text{S}{{\text{O}}_{4}}\xrightarrow{443\text{K}}{{\text{C}}_{2}}{{\text{H}}_{4}}+{{\eta }_{2}}{\mathrm O}$ So, the product formed depends on the reagents and as well as on the temperatures.Recently Updated PagesMaster Class 12 Business Studies: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Economics: Engaging Questions & Answers for Successarrow-rightMaster Class 12 English: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Maths: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Social Science: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Chemistry: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Business Studies: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Economics: Engaging Questions & Answers for Successarrow-rightMaster Class 12 English: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Maths: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Social Science: Engaging Questions & Answers for Successarrow-rightMaster Class 12 Chemistry: Engaging Questions & Answers for Successarrow-right
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