In an advanced organic chemistry laboratory, students are tasked with synthesizing a complex organic molecule \'Q\' starting from a simpler organic molecule \'P\' (CHO). The synthesis involves several steps, each incorporating a different organic reaction. The sequence of the synthesis is as follows: Compound \'P\' undergoes a Friedel-Crafts Acylation reaction with an acyl chloride under anhydrous conditions. The product of step 1 is then treated with a strong oxidizing agent to introduce an additional functional group. The oxidized product is subsequently subjected to a Wittig reaction, using a phosphonium ylide. Finally, the product of the Wittig reaction undergoes a selective catalytic hydrogenation to yield the final product \'Q\'. Based on this sequence of reactions, identify the most likely structure of compound \'Q\'. Options: A. 1-phenyl-1-propanone B. 1-phenyl-2-propanol C. 1-phenylpropene D. 1-phenylethanol Hints: Consider the initial structure of compound \'P\' and how it would change with each subsequent reaction. Remember the types of functional groups introduced or modified by each of the mentioned reactions. Think about how these functional groups and structural changes would lead to the final product \'Q\'. Don\'t use chatgpt please provide valuable answer.