Homework Answers
At first, H2SO4 protonates alcoholic oxygen.
1.
H2SO4 ------------> H+ + SO4-
There is a formation of secondory carbo cation aas intermediate. And there is a ppossibility of rearrannging itself to yield more stable trtiary carbocstion. Thus rearrangemebt happens.
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draw a step wise mechanism that illustrates how the product is
formed.
This question is worth...
Predict the product of the following reaction and draw a detailed step-wise mechanism for the transformation....
Predict the product of the following reaction and draw a
detailed step-wise mechanism for the transformation. Be sure to
show to all intermediates, formal charges, and show the movement of
electrons with curved arrows.
HA (pH 4-5)
Gradescope #2 This question is worth 10 points. The reaction between (R)-2-bromo-3-methylbutane and water in the...
Gradescope #2 This question is worth 10 points. The reaction between (R)-2-bromo-3-methylbutane and water in the presence of heat forms Br. H30* and two organic products. Draw a stepwise mechanism for this reaction, clearly showing how each product is formed. Use curved arrows to show electron movement, and include all reactive intermediates, resonance structures, etc. Br H20
Gradescope #2 This question is worth 10 points. The reaction between (R)-2-bromo-3-methylbutane and water in the...
Gradescope #2 This question is worth 10 points. The reaction between (R)-2-bromo-3-methylbutane and water in the presence of heat forms Br", H3O+ and two organic products. Draw a stepwise mechanism for this reaction, clearly showing how each product is formed. Use curved arrows to show electron movement, and include all reactive intermediates, resonance structures, etc. Br H2O Δ
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Electrophilic addition of bromine, Br-, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH2Cl2 In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product...
Draw curved arrows to show the movement of electrons in this step of the mechanism.
Electrophilic addition of bromine, Br2, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH2Cl2 In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product...
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use...
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate "acidic water"). (6 pts) 4. Draw a stepwise, detailed mechanism for the reaction below. Use curved arrows to indicate the flow of electrons. (Hint: think of this reaction as a combination of addition of HX (step 1) and hydration (step 2)]. In the second step, an...
7. Draw the structure of the organic product(s) formed in the following reaction, and propose an...
7. Draw the structure of the organic product(s) formed in the following reaction, and propose an electron-pushing mechanism for the reaction. Use arrows to clearly show the movement of electrons in each step. L E + OH + H heat - NCH₃ Mechanism: Final product(s):
4.Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the following...
4.Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the following reaction: (20 pts.) H₂ CH₂ CH,OH CH H.C. H₂C Н.С. OCH, CH, 880.
Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the following...
Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the following reaction:
Draw a detailed step-wise mechanism for the following reactions. Be sure to show all steps, formal...
Draw a detailed step-wise mechanism for the following reactions.
Be sure to show all steps, formal charges, and show the movement of
electrons with curved arrows.
MgBr 1. Со, он 2. H2O+
Predict the product of the following reaction and draw a
detailed step-wise mechanism for the transformation. Be sure to
show to all intermediates, formal charges, and show the movement of
electrons with curved arrows.
HA (pH 4-5)
Gradescope #2 This question is worth 10 points. The reaction between (R)-2-bromo-3-methylbutane and water in the presence of heat forms Br. H30* and two organic products. Draw a stepwise mechanism for this reaction, clearly showing how each product is formed. Use curved arrows to show electron movement, and include all reactive intermediates, resonance structures, etc. Br H20
Gradescope #2 This question is worth 10 points. The reaction between (R)-2-bromo-3-methylbutane and water in the presence of heat forms Br", H3O+ and two organic products. Draw a stepwise mechanism for this reaction, clearly showing how each product is formed. Use curved arrows to show electron movement, and include all reactive intermediates, resonance structures, etc. Br H2O Δ
3. Draw a stepwise, detailed mechanism for the acid-catalyzed hydration reaction in question 2 above. Use curved arrows to indicate the flow of electrons. (Note: use hydronium ion, H307, in your mechanism to indicate "acidic water"). (6 pts) 4. Draw a stepwise, detailed mechanism for the reaction below. Use curved arrows to indicate the flow of electrons. (Hint: think of this reaction as a combination of addition of HX (step 1) and hydration (step 2)]. In the second step, an...
7. Draw the structure of the organic product(s) formed in the following reaction, and propose an electron-pushing mechanism for the reaction. Use arrows to clearly show the movement of electrons in each step. L E + OH + H heat - NCH₃ Mechanism: Final product(s):
4.Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the following reaction: (20 pts.) H₂ CH₂ CH,OH CH H.C. H₂C Н.С. OCH, CH, 880.
Draw a stepwise detailed mechanism that illustrates how four organic products are formed in the following reaction:
Draw a detailed step-wise mechanism for the following reactions.
Be sure to show all steps, formal charges, and show the movement of
electrons with curved arrows.
MgBr 1. Со, он 2. H2O+
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