Please propose an experimental approach to generate a new form of chymotrypsin that is both acidophilic...
Please propose an experimental approach to generate a new form of chymotrypsin that is both acidophilic and psychrophilic.
Homework Answers
Acidophilic : ability of a substance to perform well in acidic condition and bad in basic condition.
Psychrophilic : ability of a substance to grow and reproduce in low temperature.
The New form of Chymotrypsin discussed here is : ( CHYMOTRYPSIN C ) This differs from the chymotrypsin A and B in its catalysing the hydrolysis of peptide and ester bonds at the carboxyl group of various amino acids .
Experimental approach : Here,Chymotrypsin C can be prepared from porcine pancreas glands by fractionation and chromatography on DEAE cellulose and inactive precursors of Chymotrpsin C is separated from the procarboxypeptidase A by gel filtration.
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Please propose an experimental approach to generate a new form
of chymotrypsin that is both acidophilic...
. propose a between-subjects experimental design to test the relationship. The IV and DV are already...
. propose a between-subjects experimental design to test the relationship. The IV and DV are already identified for you. Please explain how you would investigate the relationship by including: (1) your hypothesis (.e., what do you expect to happen), (2) an operational definition for your dependent variable (i.e., how will you test the variable), (3) the population (who do you want to recruit and why), (4) the levels of the IV (how many, what they are, and why), and (5)...
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Both problems please, thank you very much in
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please explain Problem 5 (10 pts) Starting from acetylene propose a synthesis of both cis-3-heptene and...
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Please Answer Both questions Propose a mechanism for the following reaction under conditions that favor a...
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Propose a mechanism for the following reaction under conditions that favor a SN1 reaction. HO -ОН Br For the following reactions provide the mechanism and explain the relative relate of the reactions. KOC(CH3)3 rel rate = 1 Br trans KOC(CH3)3 rel rate > 500 Br cis
kindly propose a synthesis form 2-butene to halomon Please make your handwritten readable and kindly explain...
kindly propose a synthesis form 2-butene to halomon
Please make your handwritten readable and kindly explain each
reaction . Thankyou for your effort ! :)
CORRECTION: FROM 2-butene to halomon
No. Halomon Co His Br2 Clz Date لم 2-butene Halomon
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What is the pretest and posttest performance of the
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Please help me.
Experimental Group n 5 PRETEST POSTTEST Control Group ။ PRETEST POSTTEST at an . က 3535 - ၁၀ 10 14 11 ထထ ထထထ ထထထ ထထ ၁၀ ) 16 14 ET EL က- 13 - 1 15 I -- ဘ = ထထထ ထ းးးးးးးးးးးးးးးးးးးးးးး 15 15 17 2. - - အ - - အ
. propose a between-subjects experimental design to test the relationship. The IV and DV are already identified for you. Please explain how you would investigate the relationship by including: (1) your hypothesis (.e., what do you expect to happen), (2) an operational definition for your dependent variable (i.e., how will you test the variable), (3) the population (who do you want to recruit and why), (4) the levels of the IV (how many, what they are, and why), and (5)...
Both problems please, thank you very much in
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3. Propose arrow.pushing mechanisms to explain the formation of each product. TOCH Emper EtMgBr LOCH, OCH och H2O H30*
Propose the mechanism please
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please explain
Problem 5 (10 pts) Starting from acetylene propose a synthesis of both cis-3-heptene and trans-3-heptene.
Please Answer Both questions
Propose a mechanism for the following reaction under conditions that favor a SN1 reaction. HO -ОН Br For the following reactions provide the mechanism and explain the relative relate of the reactions. KOC(CH3)3 rel rate = 1 Br trans KOC(CH3)3 rel rate > 500 Br cis
kindly propose a synthesis form 2-butene to halomon
Please make your handwritten readable and kindly explain each
reaction . Thankyou for your effort ! :)
CORRECTION: FROM 2-butene to halomon
No. Halomon Co His Br2 Clz Date لم 2-butene Halomon
Please do all parts.
7. Do all parts: a. Starting with benzene propose both a retrosynthesis and a stepwise synthesis for the following compound. (12 points) LOH Br b. Provide a stepwise, curved arrow mechanism points) for the following reaction. (8 AICI3
What is the pretest and posttest performance of the
learners for both experimental and control group?
Please help me.
Experimental Group n 5 PRETEST POSTTEST Control Group ။ PRETEST POSTTEST at an . က 3535 - ၁၀ 10 14 11 ထထ ထထထ ထထထ ထထ ၁၀ ) 16 14 ET EL က- 13 - 1 15 I -- ဘ = ထထထ ထ းးးးးးးးးးးးးးးးးးးးးးး 15 15 17 2. - - အ - - အ
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