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Organic Chemistry Explained's user avatar
Organic Chemistry Explained's user avatar
Organic Chemistry Explained
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24 votes

Do non-classical carbanions exist?

16 votes
Accepted

Is oxepin aromatic?

14 votes

Ipso substitution and its rules

9 votes
Accepted

How does ring size affect SN2 reactions?

5 votes
Accepted

Classification in Stereoisomerism

4 votes
Accepted

Does an acetal need to have one hydrogen attached to its carbon?

4 votes

Is benzenesulfonic acid or cyclohexanesulfonic acid more acidic?

4 votes
Accepted

How does base size affect the ratio of kinetic/thermodynamic enolate?

3 votes

What is the correct number of stereo isomers in case of 3,6-dimethylpiperazine-2,5-dione?

3 votes

What is the rate-determining step in free radical halogenation?

3 votes

Why is -OCH3 more strongly activating than -CH3 in electrophilic aromatic substitution?

3 votes
Accepted

Are the stereoisomers of nucleosides actually anomers?

3 votes

How do we determine molecule chirality in these examples?

3 votes
Accepted

Converting a thioester to an amide

3 votes

Determining R and S configuration for a cyclic compound when the lowest priority group is on the plane of the paper

2 votes

Alkali metal enolates

1 vote

Question about the mole

1 vote

Why is ammonia still considered polar despite undergoing rapid inversion?

1 vote

According to the Cahn-Ingold-Prelog system assign a priority to each of the following groups. (Highest priority is 1)