QuestionAugust 17, 2025

What is the main reason behind limited bioavailability of benzylpenicillin? The beta-lactam ring of benzy/penicillin is highly prone to acid catalyzed intermolecular hydrolysis. The beta-lactam ring of benzy/penicillin is highly prone to alkali catalyzed intermolecular hydrolysis. The beta-lactam ring of benzy/penicillin is highly prone to alkali catalyzed intramolecular hydrolysis. The beta-lactam ring of benzy/penicillin is highly prone to acid catalyzed intramolecular hydrolysis. The beta-lactam ring of benzy/penicillin is highly prone to H2O2 catalyzed intermolecular hydrolysis.

What is the main reason behind limited bioavailability of benzylpenicillin? The beta-lactam ring of benzy/penicillin is highly prone to acid catalyzed intermolecular hydrolysis. The beta-lactam ring of benzy/penicillin is highly prone to alkali catalyzed intermolecular hydrolysis. The beta-lactam ring of benzy/penicillin is highly prone to alkali catalyzed intramolecular hydrolysis. The beta-lactam ring of benzy/penicillin is highly prone to acid catalyzed intramolecular hydrolysis. The beta-lactam ring of benzy/penicillin is highly prone to H2O2 catalyzed intermolecular hydrolysis.
What is the main reason behind limited bioavailability of benzylpenicillin?
The beta-lactam ring of benzy/penicillin is highly prone to acid catalyzed intermolecular hydrolysis.
The beta-lactam ring of benzy/penicillin is highly prone to alkali catalyzed intermolecular hydrolysis.
The beta-lactam ring of benzy/penicillin is highly prone to alkali catalyzed intramolecular hydrolysis.
The beta-lactam ring of benzy/penicillin is highly prone to acid catalyzed intramolecular hydrolysis.
The beta-lactam ring of benzy/penicillin is highly prone to H2O2 catalyzed intermolecular hydrolysis.

Solution
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Answer

The beta-lactam ring of benzylpenicillin is highly prone to acid catalyzed intramolecular hydrolysis. Explanation 1. Identify the hydrolysis type Benzylpenicillin's beta-lactam ring is susceptible to acid catalyzed intramolecular hydrolysis, affecting its stability in acidic environments like the stomach.

Explanation

1. Identify the hydrolysis type<br /> Benzylpenicillin's beta-lactam ring is susceptible to acid catalyzed intramolecular hydrolysis, affecting its stability in acidic environments like the stomach.
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