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aldehydes have at least one hydrogen bond in their structure,hence they do not cause much hindrances to attacking nucleophiles.ketones on the other hand have at least 2 methyl groups attached to their structure hence,the methyl group cause steric strains hence makes it difficult for the attacking nucleophile to bond with the carbonyl carbon.in this case aldehydes wiil be able to react with nuclephiles faster than ketones.

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List of b pharmacy 1st year organic chemistry questions and answers?

I can provide you with some example questions for organic chemistry in B.Pharmacy 1st year: What is the difference between an aldehyde and a ketone? Explain the concept of chirality in organic molecules. Describe the mechanism of nucleophilic substitution. How does resonance affect the stability of organic compounds?


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The SN1 mechanism, or unimolecular nucleophilic substitution, involves two main steps. First, the leaving group departs from the substrate, forming a carbocation intermediate. This step is rate-determining and occurs independently of the nucleophile. In the second step, the nucleophile attacks the carbocation, leading to the formation of the final product. The reaction typically favors tertiary substrates due to their ability to stabilize the carbocation.


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Yes, aromatic compounds can belong to other classes of compounds. For example, they can be part of heterocyclic compounds, where the aromatic ring contains atoms other than carbon, such as nitrogen, oxygen, or sulfur. Additionally, aromatic compounds can also be functionalized to form compounds like alcohols, aldehydes, or acids while retaining their aromatic character. This versatility makes aromatic compounds integral to a wide range of chemical classes.

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