Select one activator & ortho para director to be on a benzene ring to start.  You will then add a bromine to this group showing the COMPLETE mechanism, including all resonance structures.  Put a box around the stabilizing resonance structure and explain why it is stabilizing.

Q: Identify the cyclohexyl substrate which would undergo the fastest E2 with base.

A: E2 elimination is a one step concerted mechanism reaction in which dehydrohalogenation (or any other…

Q: What is the mechanism leading to the major product? I believe this is a nucleophilic acyl…

A: In nucleophilic acyl substitution the leaving group is substituted or replaced by a nucleophile at…

Q: Select the best reagents to effect the given transformation.

A: Answer : option B is the correct answer. When aldehyde react with NaBH4 in water it will leads to…

Q: Will the following bases favor an E1 or E2 mechanism? Sort them into the appropriate boxes below.…

A: Strong base favour E-2 reaction and weak base favour E-1 reaction.

Q: What is the reagents/conditions to perform the following transformation? Problem viewing the image,…

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Q: detailed electron pushing mechanism fkr this reaction. It needs to be done as an SN2 reaction.…

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Q: Please provide a synthetic route for this molecule Br

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Q: Complete the mechanism for the given base-catalyzed formation of a hemiacetal from…

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Q: an you explain the full mechanism for this transformation

A: The aromatic substitution of hydrogen with deuterium occurs on reacting benzene with deuterated…

Q: Add any remaining curved arrows to show the two propagation steps that form the observed products.…

A: Given :  To add any remaining curved arrows to show the two propagation steps that form the observed…

Q: Provide a complete mechanism for the following reaction. Pay close attention to details, including…

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Q: The above reaction proceeds to yield only a single product. Draw the structure(s) of the…

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Q: Make one reaction scheme using proper compounds in the box below for Williamson ether synthesis.…

A: The reaction given is Williamson ether synthesis.

Q: Give one example of Williamson ether synthesis. Show the reactants materials and the product. Draw…

A: As per the multiple-question rule- I am answering the first question asked (Williamson-ether…

Q: Step 3: Add curved arrows. Select Draw Rings More Erase Select Draw Rings More Erase " CHO H. HCI…

A: Alphahydrogen containing etone enolizes to enol form which attacks on the aldehyde to produce aldol.…

Q: e Tson t

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Q: Add two curved arrows to the reactant side to illustrate the movement of electrons in the E2…

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Q: Br NaOEt ELOH

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Q: Can you help answer this problem and elaborate the steps clearly and show any reagent and…

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: Predict the product of the following substitution reaction?

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: OH Ph PhMgBr OEt Ph

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Q: Draw the major product of the reaction sequence. Omit byproducts. 1) C,H, MgBr, then H,O* 2) H, SO,,…

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Q: In the following synthesis, there are 5 steps that must be done in the correct order (i.e. Step #1,…

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Q: Propose a curved arrow mechanism for the reaction. The phenyl groups are abbreviated as "Ph" and can…

A: Alkynes on reaction with sodium in liquid ammonia give the corresponding trans alkene. The first…

Q: Find the major product, assume reagents are in excess otherwise stated.

A: It is given that an alkene is present initially undergoing reactions with the mentioned reagents,…

Q: NBs, hv CClu

A: This is a radical reaction. In the initiation step, NBS reacts with ultraviolet light light to…

Q: In the reaction shown below draw curly arrows to show how the acetylide can act as a nucleophile.

A: The following steps are involved in the attack of acetylide as a nucleophile over acetone: The…

Q: e major product of

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Q: down the product

A: Given:

Q: Construct a three-step synthesis of 3-bromo-3-methyl-2-butanol from 2-methyl-2-butene by dragging…

A: Step-1 : 3-bromo-2-methylbutan-2-ol formation Step-2 : Epoxide formation Step-3 :…

Q: For the reaction below provide all possible product(s), and circle the major product.

A: The question is based on the concept of organic reactions.   We have to identify the product formed…

Q: + HA Please write the mechanism arrows for it as an Sn1 mechanism please

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Q: Please provide mechanism (arrows, fish hook, leaving group, nuc attack,  etc.)  steps to get to the…

A: It is a problem based on radical rearrangement. Radical is formed when light falls on reactant. NBS…

Q: Sterically hindered bases produce what is the major product? Zaitsev product Hoffman…

A: In E2 elimination, when more substituted alkene is formed, it is known as Zaitsev product whereas…

Q: Show the mechanism for the following transformation HO.

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Q: Select one deactivator & meta director to be on a benzene ring to start.  You will then add a…

A: Meta director on benzene ring and it's mechanism are given below-

Q: draw out a detailed mechanism showing the transformation from stilbene to stilbene dibromide C14H12…

A: The reaction taking place is given as, => C14H12 + 2 HBr + H2O2 -------> C14H12Br2 + 2 H2O

Q: Show the mechanism for the following reaction

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Q: Determine whether the sollowing are SN1,SN2, E1, or E2 and draw the major product and if more than…

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Q: HO H, O

A: In this question, we will draw a mechanism for this reaction step by step.  Acetic anhydride is a…

Q: show mechanism please using s like Sn1 Sn2 E1 E2 رے سلHo Но

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Q: Use curved arrows to draw the mechanism of this reaction below: Hg*(OAc) +] Hg(OAc)

A: In the given reaction the alkene reacts with mercuric acetate to form a mercurinium ion…

Q: Draw the product of this mechanistic step. Ignore all lone pairs. Ignore any inorganic byproducts

A: An organic compound in which two carbon atoms are bonded to each other by a double bond is called an…

Q: React styrene oxide with sodium methoxide in methanol. Draw the product of the reaction and provide…

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Q: step by step reach to final product , give all intermediate product ) do all if u plan to do only 1…

A: Here we have to write the major product of above reaction-

Q: a) Show a detailed mechanism for the reaction to produce nitrogen gas and the two carbon radicals…

A: "Since there are multiple sub-parts in this question and it is not mentioned that which one has to…

Q: Which rearrangement product will form preferentially during the [1,2]-rearrangement of an R-group?…

A: The rearrangement product is stable if the intermediate carbocation formed is stable. We have to see…

Q: Can you please check if the reagent and intermediate are correct as well as the Meta direction

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: break down of this reaction in sequence and a complete reaction scheme

A: In the given reaction ferrocene is reacting with acetic anhydride in the presence of H3PO4 to…