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This document contains a question bank with multiple choice questions related to aldehydes, ketones, and carboxylic acids for Class 12 CBSE students. The questions cover topics like reactions of aldehydes and ketones with Grignard reagents, reactions to distinguish between structural isomers, oxidation and reduction reactions, and conversions ...
18 sty 2020 · We have compiled the NCERT MCQ Questions for Class 12 Chemistry Chapter 12 Aldehydes, Ketones, and Carboxylic Acids with Answers Pdf free download covering the entire syllabus. Practice MCQ Questions for Class 12 Chemistry with Answers on a daily basis and score well in exams.
30 mar 2023 · We have uploaded complete and comprehensive notes of Chapter 12 – Aldehydes and Ketones for chemistry FSC Part 2. You can view these class 12 chemistry chapter notes and short questions or easily download second year chemistry notes. Click the download button to download ch 12 notes in pdf format.
This set of Class 12 Chemistry Chapter 12 Multiple Choice Questions & Answers (MCQs) focuses on “Aldehydes, Ketones, and Carboxylic Acids”. These MCQs are created based on the latest CBSE syllabus and the NCERT curriculum, offering valuable assistance for exam preparation.
16 lut 2024 · Solution : (i) Cyanohydrin: Cyanohydrins are organic compounds having the formula RR′C (OH)CN, where R and R′ can be alkyl or aryl groups. Aldehydes and ketones react with hydrogen cyanide (HCN) in the presence of excess sodium cyanide (NaCN) as a catalyst to field cyanohydrin. These reactions are known as cyanohydrin reactions.
6 gru 2019 · Answer: Ammonical silver nitrate solution is called Tollen’s reagent. Uses: It is used to test aldehydes. Both aliphatic and aromatic aldehydes reduce Tollen’s reagent to shining silver mirror. It is also used to distinguish aldehydes from ketones. Question 5. Draw the structure of 3-methylbutanal. (Delhi 2011) Answer: Question 6.
25 wrz 2020 · All others are aldehydes. Among them, p-tolualdehyde is less reactive than benzaldehyde because CH 3 group present at the para position w.r.t. -CHO group will increase the electron density on the carbonyl carbon atom due to hyper conjugation effect. As a result, the nucleophile attack occurs to lesser extent as compared to benzaldehyde.
