resonance structure of acetanilide
Answers
Acetanilide
When you have a headache or muscle soreness what do you typically use to help make you feel better? Do you reach for Aleve, aspirin, or maybe Tylenol? There certainly are a lot of choices out there for over-the-counter pain management and most likely you have a particular option that works best for you and your needs.
Did you know that there's a pain medication that used to be quite common but is no longer in use? As it so happens, it's the main topic of our lesson today.
It's called acetanilide and although it used to be a commonly prescribed medication for light pain management, it quickly lost its allure among medical professionals after some serious toxicity concerns began to arise. Today, we're going to be talking about acetanilide in terms of its chemical formula, resonance structures, and some of its important derivatives. Let's get started!
Structure & Chemical Formula
Acetanilide is an organic chemical compound (meaning it's composed of carbon and hydrogen mostly) that is classified as an amide in terms of its functional group. This means that it has the carbonyl group (carbon-oxygen double bond) bonded directly to a nitrogen atom. It also contains an aromatic ring, which is a ring composed of six carbon atoms and an alternating double-single-double-single bonding pattern all around the ring.
Answer:
Below is the resonance structure for acetanilide
Explanation:
Acetanilide is a colourless, odourless solid substance that resembles a leaf or flake. It was previously known as Antifebrin and was also known as N-phenylacetamide, acetanil, or acetanilid.
The delocalization of electrons in a polyatomic ion or molecule is described by resonance structures, which are sets of Lewis structures.
Due to the presence of partial charges and fractional bonds, a single Lewis structure frequently fails to explain the bonding in a molecule/polyatomic ion. Chemical bonding is described using resonance structures in such circumstances.
