Draw the product of this elementary step in an E1cb mechanism. Use the curved arrow mechanism to determine the intermediate product formed. Include all lone pairs. Ignore stereochemistry. Ignore methanol and inorganic byproducts.

Q: Consider the nucleophilic substitution reaction shown here. (a) Argue whether this reaction takes…

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Q: Draw the mechanism and identify the product (MAJOR product only if many products are possible) if…

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Q: Draw the detailed mechanism and the product for the following reaction. Be sure to include…

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Q: Show the full curved arrow mechanism for the following reaction, clearly showing how the indicated…

A: The first step of the reaction involved the elimination of Br- (bromide) ion to generate a 2o…

Q: Draw the complete, detailed mechanism (including curved arrows) for each of the following reactions…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: H*, H20, heat NH,* + NH2 HO,

A: Applying concept of organic synthesis and reagent.

Q: Draw the complete mechanism and the major organic product for each of the following reactions.

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Q: H₂C H₂C CH3 CH₂ + NH3 + Br 4. .... + NH₂ Br Br H3C CH3 H3C Br

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Q: Please state if the substrate undergoes a carbocation rearrangement in an SN1 mechanism

A: SN1 reaction is nucleophilic substitution reaction. Rate determining step is unimolecular. SN1…

Q: Provide the step-wise mechanism for the ffg.. Draw the intermediate/s involved in each rxn. This…

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Q: Draw the complete mechanism for the reaction below, including stereochemistry.

A: H2SO4 and H2O act as dehydrating agent on double bond.  Mechanism steps  In first step, alkene…

Q: Follow the arrows and draw the intermediate and product in this reaction. Include all lone pairs.…

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Q: When Is the Mechanism E1 or E2?

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Q: Show the complete mechanism using Curved Arrow Formalism for the reaction of the compound shown…

A: INTRODUCTION: p-chlorobenzaldehyde reacts with EtOH and HCl to give an acetal.

Q: Draw the complete, detailed mechanism for the following reaction.

A: Base abstracts a hydrogen atom from CH3NO2 and it generates a good nucleophile (-CH2NO2). This…

Q: Could the reactions shown here take place by a concerted mechanism?

A: A concerted mechanism can be drawn as

Q: Identify the product of the following one-step sequence. Note that this is a reaction that you have…

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Q: show the arrows of this reaction mechanism,

A: The arrows of this reaction mechanism can be shown below The major product should show a…

Q: он Br

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Q: Use curved arrows to denote electron flow in this first step. Draw both possible carbocation…

A: In the given question an example of hydrohalogenation reaction is provided. Hydrohalogenation…

Q: Draw out the complete mechanism of the reaction and include all relevant electrons and arrows…

A: It is given that in the reaction benzaldehyde and acetone are the substrates which are undergoing a…

Q: From the cope elimination,indentify the major product for this rection and propose the mechanism to…

A: Cope elemination :-          In this reaction tertiary amine oxide undergo the elimination of a…

Q: Add curved arrow(s) to draw step 2 of the mechanism. Modify the given drawing of the product as…

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Q: Draw the mechanism for the following transformation that shows the flow of electrons leading to the…

A: Given reaction:

Q: Use Newman’s projection to predict the major product for an E2 reaction of the substrate shown…

A: Elimination reactions are those which convert saturated compound to unsaturated compounds for…

Q: Consider the following reaction scheme (note that the reagent shown above the arrow is DBN"). Draw…

A: DBN is a sterically hindered bicyclic non-nucleophilic nitrogen base.

Q: OH Ph PhMgBr OEt Ph

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Q: H2SO4 OH

A: In the given transformation one acetal bond breaks and another acetal bond is formed:

Q: Draw the mechanism for the following reaction. Be sure to include all curved arrows. HO-S-OH OH H20…

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Q: Draw the complete mechanism for this reaction. p-CH3- CgH4– SO;H + H3C-OH

A: The organic conversion helps in the conversion of one organic compound into other compounds. This is…

Q: Add curved arrow(s) to draw step 1 of the mechanism. Modify the given drawing of the product as…

A: 'O' is an electron rich species having lone pair of e- whereas H- is also an e- rich species. Both…

Q: If H1 is eliminated from the carbocation shown here in an electrophile elimination step, then three…

A: In E1 mechanism, a carbocation is formed first and then a double bond by the abstraction of proton.…

Q: Draw the mechanism for each of the following reaction. Show all steps in the reaction, the…

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Q: Draw the mechanism for the reaction of acetyl chloride (ethanoyl chloride) with the ethoxide anion…

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Q: hv D. C.

A: This is an example of 1,3-sigmatropic carbon shift followed by electrocyclic ring opening.

Q: ne mechanism proceeds through a first cationic intermediate, intermediate 1. Nucleophilie attacR…

A: We have to draw organic products

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: нн

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Q: Draw the complete mechanism and predict the products of the following Cl2 Fe or FeCl3

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Q: Br2 H20 CH3CH,CH,CCH,Br CH,CH,CH,C=CH

A: The mechanism of the following reaction is as follows:

Q: Indicate what conditions would be required for each reaction shown below in order for the overall…

A: Given reaction:

Q: Question attached

A: In substitution reaction, a carbocation intermediate is formed. Sometimes, rearrangement reaction…

Q: Follow the arrows and draw the intermediate and product in this tautomerization, Include all lone…

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Q: Draw a curly arrow mechanism to clearly describe why the following reaction gives a trans dibromo…

A: Reaction of alkenes with bromine results in the formation of vicinal dibromides i.e. 1,2-dibromides.…

Q: If H* is eliminated from the carbocation shown here in an electrophile elimination step, then three…

A: Given:

Q: HCI b.

A: First reaction involve allyl carbocation intermediate and second reaction is diels alder reaction

Q: The geometry favors the E2 mechanism because it will promote the effective

A: The leaving group is always anti-periplanar to the hydrogen that is removed on the β carbon. in…

Q: Draw this compound in a chair form so that an E2 reaction is possible. Then, draw the mechanism and…

A: E2 reaction is possible product can be drawn as,

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.