The only way of mastering any topic in Organic Chemistry is doing lots of practice problems. And I know, seeing my students, that starting to work on a practice problem may be the hardest part as you don’t know where to start. It is difficult to visualize what where the double bond would be moved if you follow the five curved arrows crammed in one step. Here is the trick:
We are always told to think before doing something. Fair enough. But let me tell you, it is also strangely enough, that in Organic Chemistry, it is often better to draw and then think about what you did (not in the lab though). It is much easier to have a structure in front of you and check for errors and improvements.
Do the first step, take the pencil and you will see that the ball gets rolling.
You have all these Organic Chemistry Practice Problems waiting to be solved!
In simple words, the Hammond postulate predicts whether the transition state resembles the reactant or the product of the reaction. According to it, the transition state resembles the structure of the species (reactant, intermediate, or product), which is closer to … Read more
Let’s start today’s discussion with simple terms: Both inductive and mesomeric (resonance) effects tell us whether one part of the molecule withdraws or donates electron density to another part of the molecule. Now, why and how does one part of … Read more
We have seen earlier that under different conditions, alkanes, alkenes, and aromatic compounds react with bromine. The halogenation of alkenes is explained by the electron-rich feature of the double bond, whereas aromatic compounds require a catalyst to make … Read more
In this chapter on alpha carbon chemistry, you are going to come across the term “enol” almost in any new reaction. So, what is an enol? As the name suggests, these are species that contain an alkene (ene) and an … Read more
In the previous few posts, we talked about the stability of aromatic compounds and the rules for determining whether a compound is aromatic or not. Aside from experimental data, the stability of aromatic compounds is also confirmed by sophisticated math … Read more
The Problems in Converting Esters to Ketones Esters are carbonyl compounds susceptible to nucleophilic additions, and one may think of converting them to ketones using Grignard, organolithium, or organocuprate reagents. However, the problem with those is that Grignard and organolithium … Read more
The sulfonation of benzene is typically achieved by reacting with fuming sulfuric acid, which is a mixture of H2SO4 and sulfur trioxide (SO3) known as oleum. The reaction follows an electrophilic aromatic substitution mechanism, producing benzenesulfonic acid. The … Read more
In today’s post, we will talk about the chlorination and bromination of benzene via electrophilic aromatic substitution. Remember, in the introductory post about aromatic compounds, we mentioned that, unlike alkenes, dienes, and other conjugated systems, benzene does not react with … Read more
Nitration of benzene or its derivatives introduces a nitro (NO2) group into the aromatic system. The reaction is carried out with a mixture of nitric and sulfuric acids at temperatures above 50 oC. The role of sulfuric acid … Read more
