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PHARMD GURU
  • Home
  • First year subjects
    • Anatomy and physiology
    • Pharmaceutics
    • Medicinal Biochemistry
    • Pharmaceutical Inorganic Chemistry
    • Pharmaceutical Organic Chemistry
    • Remedial Mathematics
  • Second year subjects
    • Pathophysiology
    • Pharmaceutical Microbiology
    • Pharmacognosy and Phytopharmaceuticals
    • Pharmacology-1
    • Community Pharmacy
    • Pharmacotherapeutics-1
  • Third year subjects
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    • Pharmaceutical Analysis
    • Pharmacotherapeutics-2
    • Pharmaceutical Jurisprudence
    • Medicinal Chemistry
    • Pharmaceutical Formulations
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    • Hospital Pharmacy
    • Clinical Pharmacy
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    • Biopharmaceutics and Pharmacokinetics
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KINETICS OF SECOND AND FIRST ORDER REACTION
  • Pharmaceutical Organic Chemistry

8. KINETICS OF SECOND AND FIRST ORDER REACTION

Kinetics of First and Second Order Reactions In organic chemistry, many reactions happen at different speeds. Some reactions finish very fast, while some take more time. The study of the…

MECHANISM AND KINETICS OF SN2 REACTIONS
  • Pharmaceutical Organic Chemistry

9. MECHANISM AND KINETICS OF SN2 REACTIONS

Mechanism and Kinetics of SN2 Reactions The SN2 reaction is a second-order nucleophilic substitution reaction. The name SN2 stands for Substitution Nucleophilic Bimolecular, meaning the rate of the reaction depends…

MECHANISM AND KINETICS OF SN1 REACTIONS
  • Pharmaceutical Organic Chemistry

10. MECHANISM AND KINETICS OF SN1 REACTIONS

Mechanism and Kinetics of SN1 Reactions The SN1 reaction is a type of nucleophilic substitution reaction. It follows first-order kinetics, meaning the reaction rate depends only on the concentration of…

1,2 elimination, E2 and E1 mechanism
  • Pharmaceutical Organic Chemistry

11. Dehydrohalogenation of alkyl halides – 1,2 elimination, kinetics, E2 and E1

Dehydrohalogenation of Alkyl Halides – 1,2 Elimination, E2 and E1 In organic chemistry, alkyl halides can undergo elimination reactions. These reactions remove two groups from a molecule and form a…

Evidence for E2 mechanism, absence of rearrangement isotope effect, absence hydrogen exchange, the element effect, orientation and reactivity
  • Pharmaceutical Organic Chemistry

12. Evidence for E2 mechanism, absence of rearrangement isotope effect, absence hydrogen exchange, the element effect, orientation and reactivity

Evidence for the E2 Mechanism E2 is a one-step elimination reaction where the base removes a β-hydrogen at the same time the leaving group leaves. Because everything happens in a…

E2 VERSUS E1, ELIMINATION VERSUS SUBSTITUTION
  • Pharmaceutical Organic Chemistry

13. E2 VERSUS E1, ELIMINATION VERSUS SUBSTITUTION

E2 VERSUS E1, ELIMINATION VERSUS SUBSTITUTION – Introduction In many organic reactions, substitution and elimination can happen at the same time. To get the correct product in synthesis, we must…

DEHYDRATION OF ALCOHOL, EASE OF DEHYDRATION, ACID CATALYSIS, REVERSIBILITY, ORIENTATION
  • Pharmaceutical Organic Chemistry

14. DEHYDRATION OF ALCOHOL, EASE OF DEHYDRATION, ACID CATALYSIS, REVERSIBILITY, ORIENTATION

Dehydration of Alcohols Dehydration means removing a molecule of water from an alcohol. When an alcohol is heated with a strong acid (like concentrated H2SO4) it loses water and forms…

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