If you like us, please share us on social media or tell your professor. Consider building or adopting a Wikitext for your course like Prof. Dianne Bennett from Sacramento City College demonstrates in this video.
Benzene was first suspected to exist way back in 1825 when British scientist Michael Faraday first isolated it from an oily mixture used in gaslights. This, and other compounds similar to it, formed a group called aromatic compounds. They were named aromatic due to their pleasing aroma, although not all smelled as such. The unusual stability of benzene makes it ideal for many reactions. Among these reactions is one known as The Friedel-Crafts Alkylation. However, the reaction suffers from a group of limitations making it a poor candidate to achieve desired results.
Friedel-Crafts Alkylation was first discovered by French scientist Charles Friedel and his partner, American scientist James Crafts, in 1877. This reaction allowed for the formation of alkyl benzenes from alkyl halides, but was plagued with unwanted supplemental activity that reduced its effectivity.
To remedy these limitations, a new and improved reaction was devised: The Friedel-Crafts Acylation, also known as Friedel-Crafts Alkanoylation.
The goal of the reaction is the following:
The very first step involves the formation of the acylium ion which will later react with benzene:
The second step involves the attack of the acylium ion on benzene as a new electrophile to form one complex:
The third step involves the departure of the proton in order for aromaticity to return to benzene:
During the third step, AlCl4 returns to remove a proton from the benzene ring, which enables the ring to return to aromaticity. In doing so, the original AlCl3 is regenerated for use again, along with HCl. Most importantly, we have the first part of the final product of the reaction, which is a ketone. Thie first part of the product is the complex with aluminum chloride as shown:
The final step involves the addition of water to liberate the final product as the acylbenzene:
Because the acylium ion (as was shown in step one) is stabilized by resonance, no rearrangement occurs (Limitation 1). Also, because of of the deactivation of the product, it is no longer susceptible to electrophilic attack and hence, is no longer susceptible to electrophilic attack and hence, no longer goes into further reactions (Limitation 3). However, as not all is perfect, Limitation 2 still prevails where Friedel-Crafts Acylation fails with strong deactivating rings.
Solution to Problem 2:
Solution to Problem 3:
Solution to Problem 4:
Solution to Problem 5: