Answer:
1) HNO3/H2SO4, 2) CH3CH2CH2Cl/AlCl3
Explanation:
Benzene is a stable aromatic compound hence it undergoes substitution rather than addition reaction.
When benzene undergoes substitution reaction, the substituent introduced into the ring determines the position of the incoming electrophile.
If I want to synthesize m-nitropropylbenzene, I will first carry out the nitration of benzene using HNO3/H2SO4 since the -nitro group is a meta director. This is now followed by Friedel Craft's alkykation using CH3CH2CH2Cl/AlCl3.
AppearanceClear, transparent and homogeneousCloudy, heterogeneous, at least two substances visibleParticle Sizemolecule in sizelarger than 10,000 AngstromsEffect of Light Tyndall Effectnone -- light passes through, particles do not reflect lightvariableEffect of Sedimentationnoneparticles will eventually settle ou
D) because both reactions are occurring at the same rate. They are not equal but their concentrations are constant.
Answer:
The pendulum would stop swinging because the kinetic energy would slow down for the friction is causing it to slow. The energy would go into potential energy.
