Answer:
The reaction would take place with racemization.
Explanation:
The compound (R)-3-bromo 3-methylhexane contains has the leaving group attached to a tertiary carbon atom. When the leaving group is attached to a tertiary carbon atom, the compound undergoes nucleophilic substitution via SN1 mechanism. This mechanism involves the formation of a planar carbocation intermediate. The nucleophile may attack this intermediate from either faces, leading to racemization of the product.
Answer: Every action force results in an equal and opposite reaction force.
Explanation: newtons law
<span> Mg(OH)2(s) + 2HCl(aq) yield MgCl2(aq) + 2H2O(l)
grams HCl required = (50.6 grams Mg(OH)2) * (1 mol Mg(OH)2 / 58.3197 grams Mg(OH)2) * (2 mol HCl / 1 mol Mg(OH)2) * (36.453 grams HCl / 1 mol HCl) = 63.26 grams HCl required
Since there are only 45.0 grams HCl, then HCl is the limiting reactant.
theoretical yield MgCl2 = (45.0 grams HCl) * (1 mol HCl / 36.453 grams HCl) * (1 mol MgCl2 / 2 mol HCl) * (95.211 grams MgCl2 / 1 mol MgCl2) = 58.6 grams MgCl2 </span>
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