For each compound, 1. name the functional group. 2. show what compound(s) result from complete hydrolysis. (g)
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Step 1: Identify the functional group in the compound. The structure provided is a heterocyclic compound with two nitrogen atoms in a six-membered ring. This functional group is classified as a diazine, specifically 1,4-diazine (also known as pyridazine).
Step 2: Understand the concept of hydrolysis. Hydrolysis typically involves breaking chemical bonds in the presence of water, often targeting ester, amide, or glycosidic bonds. However, in this case, the compound does not contain hydrolyzable bonds like esters or amides.
Step 3: Analyze the structure for potential hydrolysis products. Since the compound is a stable aromatic heterocycle, hydrolysis under normal conditions would not break the ring structure. No hydrolysis products are expected unless extreme conditions are applied.
Step 4: Consider the chemical stability of the compound. Pyridazine is resistant to hydrolysis due to its aromaticity and lack of hydrolyzable functional groups.
Step 5: Conclude that under complete hydrolysis conditions, no new compounds are formed because the structure lacks hydrolyzable bonds. The compound remains unchanged.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Functional Groups
Functional groups are specific groups of atoms within molecules that are responsible for the characteristic chemical reactions of those molecules. They determine the properties and reactivity of organic compounds. Common functional groups include hydroxyl (-OH), carboxyl (-COOH), and amine (-NH2), each imparting distinct behaviors to the compounds they are part of.
Hydrolysis is a chemical reaction involving the breaking of a bond in a molecule using water. In organic chemistry, it often refers to the reaction of a compound with water to form two or more products. Complete hydrolysis typically results in the breakdown of larger molecules, such as esters or amides, into their constituent parts, such as acids and alcohols.
Naming organic compounds follows specific rules set by the International Union of Pure and Applied Chemistry (IUPAC). This systematic approach includes identifying the longest carbon chain, naming the functional groups, and assigning locants to indicate the position of substituents. Proper naming is essential for clear communication in chemistry, ensuring that each compound can be accurately identified and understood.