Wear safety goggles when conducting chemistry experiments. Add aqueous bromine to compound F to test for an alkene, indicated by the solution turning colorless. Prepare Tollens' reagent by mixing aqueous silver nitrate and sodium hydroxide, then add it to compound A to identify carbonyl groups, shown by a silver mirror forming. Test for phenol by adding ammonia solution to compound D with iron(III) chloride, seen by a purple color. Identify primary or secondary alcohols by compound E turning from orange to green with acidified potassium dichromate. Carbonic acid is compound B, reacting with sodium carbonate to release carbon dioxide seen as fizzing.
Wear safety goggles when conducting chemistry experiments. Add aqueous bromine to compound F to test for an alkene, indicated by the solution turning colorless. Prepare Tollens' reagent by mixing aqueous silver nitrate and sodium hydroxide, then add it to compound A to identify carbonyl groups, shown by a silver mirror forming. Test for phenol by adding ammonia solution to compound D with iron(III) chloride, seen by a purple color. Identify primary or secondary alcohols by compound E turning from orange to green with acidified potassium dichromate. Carbonic acid is compound B, reacting with sodium carbonate to release carbon dioxide seen as fizzing.
Wear safety goggles when conducting chemistry experiments. Add aqueous bromine to compound F to test for an alkene, indicated by the solution turning colorless. Prepare Tollens' reagent by mixing aqueous silver nitrate and sodium hydroxide, then add it to compound A to identify carbonyl groups, shown by a silver mirror forming. Test for phenol by adding ammonia solution to compound D with iron(III) chloride, seen by a purple color. Identify primary or secondary alcohols by compound E turning from orange to green with acidified potassium dichromate. Carbonic acid is compound B, reacting with sodium carbonate to release carbon dioxide seen as fizzing.
Wear safety goggles when conducting chemistry experiments. Add aqueous bromine to compound F to test for an alkene, indicated by the solution turning colorless. Prepare Tollens' reagent by mixing aqueous silver nitrate and sodium hydroxide, then add it to compound A to identify carbonyl groups, shown by a silver mirror forming. Test for phenol by adding ammonia solution to compound D with iron(III) chloride, seen by a purple color. Identify primary or secondary alcohols by compound E turning from orange to green with acidified potassium dichromate. Carbonic acid is compound B, reacting with sodium carbonate to release carbon dioxide seen as fizzing.
Wear goggles in order to conduct the experiment safely.
To test for a C C (alkene) functional group add a few drops of aqueous bromine to the compound F. The colour will change from orange to colourless. Then prepare tollens by adding aqueous NaOH to aqueous AgNo . The tollens reagent will be used to identify the C O functional group. Add this to compound A. A silver mirror is found as a result of a positive test. To identify the phenol, ad 2mol/dm NH solution to iron (III) Chloride. Phenols cause a purple colour. This should be D. The primary or secondary alcohol will go from orange to green with the addition of acidified potassium dichromate. This shows an O-H group. This is compound E. The carboxylic acid will react with sodium carbonate to liberate CO . This is observed by fizzing and highlights the presence of C O functional group. This should be compound B. This means that the remaining compound is C as every other compound has been determined.