WebCompound A gives a precipitate with alcoholic AgNO,, so it must contains Br in side chain. On oxidation, it gives $C_8H_6O_4$, which shows the presence of two alkyl ... WebClick here👆to get an answer to your question ️ Compound (A), C8H9Br , gives a pale yellow colour precipitate, when warmed with alcoholic AgNO3 . Oxidation of (A) gives a …
Compound (A), C8H9Br, gives a white precipitate when warmed …
WebAug 15, 2024 · Antimony (Sb³⁺) To 10 drops of solution, add 6 M NH 3(aq) until neutral. Make the solution acidic by adding one or more drops of 6 M HCl. Add 1 mL of thioacetamide and stir well. Heat the test tube in the boiling water bath for 5 minutes. If antimony is present, a red orange precipitate of antimony sulfide should form. WebCompound (A), C8H9Br , gives a white precipitate when warmed with alcholic AgNO3 . Oxidation of (A) gives an acid (B), C8H6O4. (B) easily forms anhydride on heating. top gear car homes
Compound (A), C8H9Br, gives a white precipitate - esaral.com
WebClick here👆to get an answer to your question ️ JUDITUUUU133CUI (d) CH3CH2Cl>CH3Cl>(CH3)2CHCI>(CH3)2CCI Compound (A), C8H9Br, gives a yellow precipitate wh ives a yellow precipitate when warmed with alcoholic AgNO3. an acid (B), C8H04.(B) easily forms anhydride on heating. Identify the Oxidation of (A) gives an acid … WebThese 4 benzylic hydrogen will give peak around 7 and will give doublet while the ethyl group will give triplet and quartet . 2) ... The 1H NMR spectrum of a compound (C8H9Br) produces the following 'H NMR data: 7.36 5 (doublet, 2H), 7.03 5 (doublet, 2H), 2.56 8 (quartet, 2H) & 1.19 (triplet, 3H). Propose a structure for the compound. 2. How ... WebPrevious Question: An organic compound A upon reacting with NH3 gives B. On heating, B gives C. C in presence of KOH reacts with Br2 to give CH3CH2CH2. A is - Next Question: A compound with molecular mass 180 is acylated with CH3COCl to get a compound with molecular mass 390. The number of amino groups present per molecule of the former ... picture of search warrant