1. The student conducted experiments to study the reactions of aliphatic and aromatic hydrocarbons with bromine and potassium permanganate.
2. In the bromine experiment, cyclohexane, cyclohexene and toluene were reacted with bromine in dichloromethane under sunlight and in the dark. Cyclohexene and toluene reacted with bromine in both conditions but cyclohexane only reacted in sunlight.
3. In the oxidation experiment, the three hydrocarbons were reacted with alkaline potassium permanganate. Only cyclohexene was decolored, showing it contains a double bond.
1. The student conducted experiments to study the reactions of aliphatic and aromatic hydrocarbons with bromine and potassium permanganate.
2. In the bromine experiment, cyclohexane, cyclohexene and toluene were reacted with bromine in dichloromethane under sunlight and in the dark. Cyclohexene and toluene reacted with bromine in both conditions but cyclohexane only reacted in sunlight.
3. In the oxidation experiment, the three hydrocarbons were reacted with alkaline potassium permanganate. Only cyclohexene was decolored, showing it contains a double bond.
1. The student conducted experiments to study the reactions of aliphatic and aromatic hydrocarbons with bromine and potassium permanganate.
2. In the bromine experiment, cyclohexane, cyclohexene and toluene were reacted with bromine in dichloromethane under sunlight and in the dark. Cyclohexene and toluene reacted with bromine in both conditions but cyclohexane only reacted in sunlight.
3. In the oxidation experiment, the three hydrocarbons were reacted with alkaline potassium permanganate. Only cyclohexene was decolored, showing it contains a double bond.
1. The student conducted experiments to study the reactions of aliphatic and aromatic hydrocarbons with bromine and potassium permanganate.
2. In the bromine experiment, cyclohexane, cyclohexene and toluene were reacted with bromine in dichloromethane under sunlight and in the dark. Cyclohexene and toluene reacted with bromine in both conditions but cyclohexane only reacted in sunlight.
3. In the oxidation experiment, the three hydrocarbons were reacted with alkaline potassium permanganate. Only cyclohexene was decolored, showing it contains a double bond.
EXPERIMENT 4: REACTIONS OF ALIPHATIC AND AROMATIC HYDROCARBONS
DARREN LEE HUA EE
MS2225208152
K2T4A
Objectives 1. To study the chemical properties of an alkane, alkene and arene.
2. To differentiate an alkene from an alkene and arene. Introduction Hydrocarbons are organic compounds that contain only carbon and hydrogen. Alkanes which are also known as paraffins are saturated hydrocarbons. They do not contain douoble and triple bonds. Hence, alkenes are relatively inert to chemical reactions.
Alkenes are unsaturated hydrocarbons with at least one double bond between 2 carbonatoms.
Alkenes undergo electrophilic addition reactions ar the 𝐶 = 𝐶 bond. For example,
alkenes undergo hydrogenation and halogenation to form alkanes and dihalides, respectively. Chemical Reaction:
Procedure of 1. 6 dry, clean test tubes were labelled, A to F.
Part (A): 2. 1ml of cyclohexane in test tubes A and B, 1ml of cyclohexene in test tubes Reaction with C and D and 1ml of toluene in test tubes E and F were placed. Bromine in 3. Test tubes A, C and E were wrapped with black sugar papers. Dichloromethane 4. 4 to 5 drops 4% bromine in dichloromethane were added into each test tube. 5. Test tubes A, C and E were kept in a dark place and test tubes B, D and F were kept in the sunlight. They were left for 15 minutes. 6. The observations were observed. Procedure of 1. Dry, clean test tubes G, H and I were labelled. Part (B): 2. 1ml each of cyclohexane, cyclohexene and toluene were placed in test Oxidation with tubes G, H and I respectively. Cold Alkaline 3. A few drops of alkaline 𝐾𝑀𝑛𝑂4 solution was added into each test tube Solution of and shaken. 𝐾𝑀𝑛𝑂4 4. The observations were recorded. (Baeyer’s Test) Results and Tabulation Hydrocarbons Bromine in Dichloromethane Oxidation with Under sunlight In the dark alkaline 𝐾𝑀𝑛𝑂4 (Baeyer’s Test) Cyclohexane The reddish The reddish The purple colour brown colour of brown colour of of 𝐾𝑀𝑛𝑂4 bromine turned bromine remained colourless. remained unchanged. unchanged. Cyclohexene The reddish The reddish The purple colour brown colour of brown colour of of 𝐾𝑀𝑛𝑂4 turned bromine turned bromine turned into brown colourless. colourless. colour. Toleune The reddish The reddish The purple colour brown colour of brown colour of of 𝐾𝑀𝑛𝑂4 bromine turned bromine remained colourless. remained unchanged. unchanged.
Discussion Reasons of Errors:
1. The test tubes with black sugar paper is not quickly placed into the cupboard. 2. Some sunlight can penetrate into the cupboard. Precautionory Steps: 1. The bromine in handled in the fume chamber. 2. Mask and gloves should be wore. Questions 1. Write the mechanism for the reaction of cyclohexane with bromine.
2. State the function of sunlight in Part (B).
Provides energy for the homolytic cleavage of halogen. Conclusion From this experiment, 1. The chemical properties of an alkane, alkene and arene were able to be studied. 2. An alkane was able to be differentiated from an alkene and arene.