Draw the structure(s) of the major organic product(s), including counterions, of the following reaction.CH3요OH•You do not have to consider stereochemistry.• Include counter-ions, e.g., Na+, I, in your submission, but draw them in their own separate sketcher.•If no reaction occurs, draw the organic starting material.••Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.Separate multiple products using the + sign from the drop-down menu.ChemDoodleⓇ?<>

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Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter16: Synthesis Workshop 1

Section: Chapter Questions

Problem 10CTQ

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Draw the organic product(s) of the following reaction. You do not have to consider stereochemistry. Include cationic counter-ions, e.g., Na+ in your answer, but draw them in their own sketcher. If no reaction occurs, draw the organic starting material. Separate multiple products using the + sign from the drop-down menu.
draw the product of the reaction shown below. Use wedge and dash bonds to indicate stereochemistry where appropriate. Ignore inorganic byproducts.
Assume that 2-chloropropane reacts with CN− in an SN2 reaction. Use the JSME editor () to draw the structure of the substitution product of the reaction. The guide on how to draw your structure can be found here Important Note: When drawing the structures in the JME editor please adhere to the following formats: 1. If the nucleophile is OH−, DO NOT manually add the "H" to the final product 2. If the nucleophile is CN−, be sure to include the appropriate bonding between the C and N in the final product
Rearrangements can occur during the dehydration of 1° alcohols even though no 1° carbocation is formed—that is, a 1,2-shift occurs as the C— OH2+ bond is broken, forming a more stable 2° or 3° carbocation, as shown in Equation [1]. Using this information, draw a stepwise mechanism for the reaction shown in Equation [2]. We will see another example of this type of rearrangement in Section 16.5C.
Several reagents and several organic structures are shown below. Construct a multistep synthetic route from the reactant 2-methyl-1-butene to the product 3-bromo-2-methyl-2-butanol by dragging the appropriate pieces into the bins. Note that each bin will hold only one item, and not every given reagent or structure will be used.
Please help with the attached OChem reaction. Fill in the correct reagents, provide the stepwise mechanism for both step 1 and 2, and include the correct use of arrows showing the flow of electrons. Thanks!
Construct a multistep synthetic route from ethylbenzene to (2-bromoethyl)benzene by dragging the appropriate items into the bins. Note that each bin will hold only one item, and not all reagents and structures will be used.
Alcohols react with sulfonyl chlorides to form sulfonate esters. Only the O-H bond of the alcohol is broken in the reaction, and so no inversion of configuration occurs. The resulting sulfonate esters are reactive in SN1 and SN2 reactions since the sulfonate group is a very weak base and is therefore a good leaving group.Draw curved arrows to show the movement of electrons in this step of the mechanism.
Rearrangements can occur during the dehydration of 1° alcohols eventhough no 1° carbocation is formed—that is, a 1,2-shift occurs as the C—OH2+ bond is broken, forming a more stable 2° or 3° carbocation, asshown in Equation [1]. Using this information, draw a stepwisemechanism for the reaction shown in Equation [2]. We will see anotherexample of this type of rearrangement
In parts 1 and 2 draw the two organic products of this reaction, showing any nonzero formal charges. Then, in part 3 answer the question regarding purification of the reaction mixture. 1. Draw the product with the higher molecular weight here: 2. Draw the product with the lower molecular weight here:
a. Write the complete mechanism, step by step, for the reaction shown in the image A, in such a way that it explains the formation of the products (Please do not forget the correct use of arrows!). b. Write the complete mechanism (suppose an E2), step by step of the reaction shown in the figure B, in such a way that it explains the formation of a single product (DO NOT FORGET THE CORRECT USE OF THE ARROWS!). Using structures, justify the formation of the chosen product and not others. c. Write the complete mechanism (suppose a bimolecular reaction), step by step of the reaction shown in the figure C, in such a way that it explains the formation of all possible products (there are three). (DON'T FORGET TO USE THE ARROWS CORRECTLY!). Watch out for stereochemistry!
Can someone help me with these and explain how they did it? The question is to predict the major organic product of each reaction.

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