Try it on paper first. A hint, the key idea and the worked solution are here when you need them.
A sample of of propene is treated with excess hydrogen bromide gas in the absence of a peroxide. Take for propene and for . One mole of gas occupies at standard temperature and pressure. The reaction goes with yield. Find the amount of propene, the volume of hydrogen bromide gas the reaction needs at standard temperature and pressure, and the mass of 2-bromopropane obtained.
In free radical halogenation the share of a product is proportional to the number of hydrogen atoms times their reactivity. Bond enthalpies give the energy change of a step: bonds broken minus bonds formed. Hydrogen halides add to alkenes by Markovnikov's rule, and an alcohol with NaBr and sulphuric acid gives a bromoalkane.
Have you tried it?
Work it out on paper first. It is fine to get stuck or make a mistake: that is how we learn. When you are ready, go through the solution one step at a time, and check each step against your own.
Plan. Use the 1 : 1 ratio of propene to hydrogen bromide, then apply the yield.
Step 1. Propene. .
Step 2. Hydrogen bromide. The ratio is 1 : 1, so is needed: .
Step 3. Product. Hydrogen adds to the carbon that already has more hydrogen atoms, and bromine goes to the middle carbon. The product is 2-bromopropane. Theoretical mass: . At : .
Answer: of propene, of hydrogen bromide and of 2-bromopropane.
Watch out. With a peroxide the product would be 1-bromopropane, of the same molar mass. The mass would be the same and the compound different.
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