Please explain along with showing the mechanism. I am thinking this
one has to do with the reaction favoring x due to better
carbocation stability but I am unsure.Homework Answers
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Please explain along with showing the mechanism. I am thinking this
one has to do with...
I do not understand how to do this, can i please have a step by step...
I do not understand how to do this, can i please have a step by
step explanation for each part
The pka of HI = -10, and for CH3OH = 16. Use these values to determine which direction the following reaction will proceed. Explain your answer based on the strength/stability of the Lewis Base. CH3CH2-1 + OCH3 = CH3CH2OCH3 + 10 Circle the better leaving group in each of the following pairs. Explain your answer using terms such as charge,...
please Answer in Details showing all the steps. Thank you Look at the following reaction: Toluene...
please Answer in Details showing all the steps.
Thank you
Look at the following reaction: Toluene OH + CH3OH OCH3 + H2O a) What is the effect of each of the given changes (see next page) on the rate of the reaction? The possible answers are: Increases, decreases, remains the same or no more reaction. 1- Decreasing the concentration of CH,OH 2-Using a Dean-Stark apparatus (used to remove water from the reaction mixture) 3- Adding H,SO, to the reaction mixture...
I have gotten these wrong a few times when given a reaction bank but, I do...
I have gotten these wrong a few times when given a reaction bank
but, I do not have a reaction bank and would like step by step help
with the question below. I attempted a few times but, I am not
coming up with the product.
I want you to devise a synthetic route for the molecule shown below. Think through the steps, what should you do first and why. Draw your answer, showing each intermediate along the route, so...
explain how i am suppose to do these i need major help thxs!! Homework #4 Due...
explain how i am suppose to do these i need major help thxs!!
Homework #4 Due Monday March 9, 2020 Problem 1: Draw the direct Newman projections of the following molecules, along the indicated bond. Then Draw the most stable and the least stable conformation. CH3 Most Stable Least stable Direct I TOH HT XH OH CH3 Direct Most Stable Least stable OH 92 Problem V: Critical Thinking One of the formation of an epoxide in a cyclohexane is by...
Please help with the question that I have circled in red. This is from a lab...
Please help with the question that I have circled in red. This
is from a lab I did and I have included the entire handout in case
it helps you to answer the question.
2015 Chem 263 2-Credit Org Lab 6T: Dehydration of Cyclohexanol to Cyclohexene Lab 6T w lecture you recently learned that alkenes undergo acid-catalyzed addition of H20 (hydration of the alkene) to yield alcohols. This lab with illustrate the same chemistry in reverse; the microscopic reverse of...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
Please make sure your answer is correct. I have gotten numerous wrong answers. Thanks. This one...
Please make sure your answer is correct. I have gotten numerous
wrong answers. Thanks.
This one too:
And this one:
Again please make sure you are correct.
If you have time: This one was marked wrong too, so if you can
solve I give thumbs up thanks.
Consider the following reaction mechanism: Step 1 K 2A + B =D (fast equilibrium) Step 2 D+B *3 E+F (slow) Step 3 FKG (fast) c. What is the rate law that corresponds to...
need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an A...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
how do i calculate the number of moles, theoretical yield, and limiting reagent on the READ...
how do i calculate the number of moles, theoretical yield, and
limiting reagent on the READ ABOUT part? thank you
i need help on READ ABOUT: Calculate the number of moles of
2-methyl-2-butanol and hydrochloric acid (concentrated HCl is 12
M). Based on the balanced equation, determine the limiting reagent
and the theoretical yield of 2-chloride-2-methylbutane.
PREPARATION AND ANALYSIS OF T-AMYL CHLORIDE ОН HCI (conc.) + H2O DISCUSSION: Compounds with good leaving groups often participate in substitution reactions. Two limiting...
i need help with this lab please. can i get someone to answer the entire thing....
i need help with this lab please. can i get someone to answer
the entire thing. thank you
Instructor Equilibria of Coordination Compounds OBSERVATIONS AND DATA 1. The formation of complex ions with ammonia The net ionic equation for the reaction of excess Cuso, with NH, is 24 Cu2+ + 4NH3 [cu (NH3)4] The predicted effect on the reaction above of adding excess NH, (based on Le Châtelier's principle) is The reaction will shift to the night and product formation...
I do not understand how to do this, can i please have a step by
step explanation for each part
The pka of HI = -10, and for CH3OH = 16. Use these values to determine which direction the following reaction will proceed. Explain your answer based on the strength/stability of the Lewis Base. CH3CH2-1 + OCH3 = CH3CH2OCH3 + 10 Circle the better leaving group in each of the following pairs. Explain your answer using terms such as charge,...
please Answer in Details showing all the steps.
Thank you
Look at the following reaction: Toluene OH + CH3OH OCH3 + H2O a) What is the effect of each of the given changes (see next page) on the rate of the reaction? The possible answers are: Increases, decreases, remains the same or no more reaction. 1- Decreasing the concentration of CH,OH 2-Using a Dean-Stark apparatus (used to remove water from the reaction mixture) 3- Adding H,SO, to the reaction mixture...
I have gotten these wrong a few times when given a reaction bank
but, I do not have a reaction bank and would like step by step help
with the question below. I attempted a few times but, I am not
coming up with the product.
I want you to devise a synthetic route for the molecule shown below. Think through the steps, what should you do first and why. Draw your answer, showing each intermediate along the route, so...
explain how i am suppose to do these i need major help thxs!!
Homework #4 Due Monday March 9, 2020 Problem 1: Draw the direct Newman projections of the following molecules, along the indicated bond. Then Draw the most stable and the least stable conformation. CH3 Most Stable Least stable Direct I TOH HT XH OH CH3 Direct Most Stable Least stable OH 92 Problem V: Critical Thinking One of the formation of an epoxide in a cyclohexane is by...
Please help with the question that I have circled in red. This
is from a lab I did and I have included the entire handout in case
it helps you to answer the question.
2015 Chem 263 2-Credit Org Lab 6T: Dehydration of Cyclohexanol to Cyclohexene Lab 6T w lecture you recently learned that alkenes undergo acid-catalyzed addition of H20 (hydration of the alkene) to yield alcohols. This lab with illustrate the same chemistry in reverse; the microscopic reverse of...
250 ChemActivity 29 Electrophilic Aromatic Substitution no ChemActivity 29 Part A: Electrophilic Aromatic Substitution (What products are formed when a strong electrophile is added to benzene?) Model 1: (review) Electrophilic Addition of HCI Rani o g cyclohexene carbocation intermediate Run 2 U X benzene This product carbocation intermediate DOES NOT Critical Thinking Questions 1 For Rxn I (above) draw curved arrows showing the mechanism of electrophilic addition of HCl. Include an appropriate carbocation intermediate in the box above. Figure 1:...
Please make sure your answer is correct. I have gotten numerous
wrong answers. Thanks.
This one too:
And this one:
Again please make sure you are correct.
If you have time: This one was marked wrong too, so if you can
solve I give thumbs up thanks.
Consider the following reaction mechanism: Step 1 K 2A + B =D (fast equilibrium) Step 2 D+B *3 E+F (slow) Step 3 FKG (fast) c. What is the rate law that corresponds to...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
how do i calculate the number of moles, theoretical yield, and
limiting reagent on the READ ABOUT part? thank you
i need help on READ ABOUT: Calculate the number of moles of
2-methyl-2-butanol and hydrochloric acid (concentrated HCl is 12
M). Based on the balanced equation, determine the limiting reagent
and the theoretical yield of 2-chloride-2-methylbutane.
PREPARATION AND ANALYSIS OF T-AMYL CHLORIDE ОН HCI (conc.) + H2O DISCUSSION: Compounds with good leaving groups often participate in substitution reactions. Two limiting...
i need help with this lab please. can i get someone to answer
the entire thing. thank you
Instructor Equilibria of Coordination Compounds OBSERVATIONS AND DATA 1. The formation of complex ions with ammonia The net ionic equation for the reaction of excess Cuso, with NH, is 24 Cu2+ + 4NH3 [cu (NH3)4] The predicted effect on the reaction above of adding excess NH, (based on Le Châtelier's principle) is The reaction will shift to the night and product formation...
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