consider the pair of solvolysis reactions. draw the organic products, then predict the type of substitution mechanism and compare the expected rates. both reactions start with a carbon bonded to three methyl groups and a chloride ion at a concentration of 1.5 molar. each reacts with methanol at 5 degrees celsius to give the product. reaction 1 has 30 milliliters of the methanol, while reaction 2 has 60 milliliters of the methanol. draw product 1. draw product 2. identify the mechanism of each reaction. reaction 2 occurs by an sn2 mechanism. reaction 1 occurs by an sn2 mechanism. reaction 2 occurs by an sn1 mechanism. reaction 1 occurs by an sn1 mechanism. compare the rates of each reaction. reaction 2 is faster than reaction 1. both reactions occur at the same rate. reaction 1 is faster than reaction 2.