{"@context":"https://schema.org/","@type":"Quiz","dateCreated":"2025-04-29T09:04:01.441Z","dateModified":"2025-11-26T04:29:23.766Z","typicalAgeRange":"11-18","educationalLevel":"MHT CET","assesses":"Chemistry - Aromatic Substitution Reactions","educationalAlignment":[{"@type":"AlignmentObject","alignmentType":"educationalTopic","targetName":"Aromatic Substitution Reactions"},{"@type":"AlignmentObject","alignmentType":"educationalSubject","targetName":"Chemistry"},{"@type":"AlignmentObject","alignmentType":"educationalExam","targetName":"MHT CET"}],"name":"Quiz about Aromatic Substitution Reactions","about":{"@type":"Thing","name":"Chemistry - Aromatic Substitution Reactions"},"hasPart":[{"@type":"Question","eduQuestionType":"Multiple choice","learningResourceType":"Practice problem","educationalLevel":"intermediate","name":"Question About Aromatic Substitution Reactions","text":"What is the product obtained on the reaction of chlorobenzene with concentrated HNO3?}","encodingFormat":"text/markdown","comment":{"@type":"Comment","text":"When working with aromatic substitution reactions, remember that the position of substitution is influenced by the nature of the substituent on the ring. Chlorine, being an electron-donating group, directs substitution to the ortho and para positions."},"suggestedAnswer":[{"@type":"Answer","position":0,"encodingFormat":"text/markdown","text":"

Para nitro chloro benzene \n

","comment":{"@type":"Comment","text":"\"\""}},{"@type":"Answer","position":1,"encodingFormat":"text/markdown","text":"

Ortho nitro chloro benzene \n

","comment":{"@type":"Comment","text":"\"\""}},{"@type":"Answer","position":2,"encodingFormat":"text/markdown","text":"

Mixture of ortho and para nitro benzene \n\n

","comment":{"@type":"Comment","text":"\"\""}},{"@type":"Answer","position":3,"encodingFormat":"text/markdown","text":"

","comment":{"@type":"Comment","text":"\"\""}}],"acceptedAnswer":{"@type":"Answer","position":2,"encodingFormat":"text/markdown","text":"

Mixture of ortho and para nitro benzene \n\n

","comment":{"@type":"Comment","text":"When working with aromatic substitution reactions, remember that the position of substitution is influenced by the nature of the substituent on the ring. Chlorine, being an electron-donating group, directs substitution to the ortho and para positions."},"answerExplanation":{"@type":"comment","text":""}}}]}

What is the product obtained on the reaction of chlorobenzene with concentrated HNO3?

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