A) The biotransformation of this drug: Choose all that apply. CH3 CH3 H,c-N. OH H,C OH он HO H,C. Phase I Phase II Reductive reaction Oxidative reaction Hydrolysis reaction glucuronic acid conjugation sulfate conjugation O methylation O acetylation product becomes less water soluble Porducts become more water soluble excretion of the products mostly happens in kidney excretion of the product mostly happens in feces B) What is the enzyme and coenzyme/cosubsrate ?

A) The biotransformation of this drug: Choose all that apply. CH3 CH3 H,c-N. OH H,C OH он HO H,C. Phase I Phase II Reductive reaction Oxidative reaction Hydrolysis reaction glucuronic acid conjugation sulfate conjugation O methylation O acetylation product becomes less water soluble Porducts become more water soluble excretion of the products mostly happens in kidney excretion of the product mostly happens in feces B) What is the enzyme and coenzyme/cosubsrate ?

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

What is the function of lyases? a. to catalyze redox reactions b. They catalyze reactions in which H₂O, NH3 and CO2 groups are removed c. They catalyze hydrolysis reactions. D. transfer active groups
Part III: Mechanism of acid-catalyzed ester hydrolysis Consider the following six-step reaction when answering the questions below: :0: R--CH₂ + Step 1: Ester protonation 10: H₂O 4. The first step in this reaction mechanism uses the acid catalyst to protonate the ester. a. Which site on the ester is the most basic and therefore most likely to gain the proton? To help answer this question draw the conjugate acid that would result from protonation of either site and explain which conjugate acid is more stable.
Shown below is the structure of the fatty acid, lauric acid. H3C CH₂ _CH 2 CH2 CH2 CH 2 CH₂ CH2 CH₂ CH2 OH CH₂ C The boxed portion is considered to be both Opolar and hydrophilic Ohydrophilic and hydrophobic Opolar and hydrophobic nonpolar and hydrophilic nonpolar and hydrophobic
B) Which of the compounds pictured could be identified as one controlling the development of the sex organs and secondary sexual characteristics? Would it react with NaBH4? Explain why or why not.
1. Fill in the boxes to complete the reaction below: LIAIH4, THF
Chemistry Question
2. What type of chemical reaction is illustrated by the following reaction? CH3OOCH3 + H2O ⎯→ CH3OOH + CH3OH a. oxidation/reduction b. substitution c. neutralization d. hydrolysis e. dehydration synthesis (condensation)
Identify the reaction type. a. dehydration b. hydrolysis (in acid) c. amide synthesis d. esterification e. hydration f. hydrolysis (in base) g. acid base
5. Identify all hydrolytic products from the following. Ph cat. H3O* PhO, H20 1 OCH3
(c) Draw the reagents needed to produce CH3CH₂CH₂OD Draw Your Solution
Take a look at this organic reaction: CH3- 0=0 C O NAD+ NADH CH₂_1-0 CH3—C−O + CO2 The reactant molecule is re-drawn in the drawing area below. Highlight in red any groups in this molecule in which carbon atoms are oxidized by the reaction. Highlight in blue any groups in which carbon atoms are reduced. If no carbon atoms are oxidized or reduced, check the box under the drawing area. _L_L- C CH₂ - No carbons are oxidized or reduced. Ć
Please don't provide handwriting solution