CH3OH Sy1 Br

Q: How does an SN1 reaction mechanism form answers A and C?

A: The question is based on the concept of organic reactions. we need to explain the product formation…

Q: Draw the major product from this reaction. Use wedge and dash bonds to indicate relative…

A: Stereochemistry of this reaction is controlled by the methyl group, which is present above the…

Q: Which one is the most elecrophilic which one is the least electrophilic

A: There are some factors which directly affects the electrophilicity of the carbonyl group. Mesomeric…

Q: Br > DBN > Ez Reaction

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: Predict the starting alkyl bromide that would produce the product shown in the SN1 reaction. Assume…

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Q: AICI Br ?

A: In the given question, a reaction is given with reagent and reactant. We have to find the major…

Q: Draw the major organic product for the reaction. Do not draw byproducts. Be sure to specifically…

A: In NaCN , CN- acts as a strong nucleophile and attack to the carbon containing leaving group OTs .

Q: OCHS H,C-S но 1 4 3.

A: The leaving group ability of a species depends on the stability of the anion. As the stability of…

Q: For the following dehydrohalogenation (E2) reaction, draw the major organic product(s), including…

A: E2 is a bimolecular reaction. The reaction involves one step mechanism in which the carbon –hydrogen…

Q: Predict the starting alkyl bromide that would produce the product shown in the SN1 reaction. Assume…

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Q: None

A: In an E2 mechanism which refers to bimolecular elimination is basically a one-step mechanism.Here,…

Q: Which of the following is the poorest leaving group in SN1 reactions? A) -OH B) -I с -F (D) None of…

A: ->The conjugate base of strong acid is good leaving group. Order of acidity -> HI > HF >…

Q: A) Please provide a mechanism for the following transformations to the final product. 1) NaOEV EIOH…

A: As per our guidelines I  can answer only first question because you have posted multiple questions.…

Q: Show how the following compound can be synthesized (made) using two different alkenes (two different…

A: Tertiary carbocation is most stable.

Q: Draw the product of the following reaction, including stereochemistry. H OTs Na* "OCH,CH3

A: When compound OTs are treated with base NaOCH2CH3 then elimination reaction occur.  The reaction…

Q: Rank the following aromatic rings from the slowest to the fastest rate of electrophilic aromatic…

A: Aromatic compounds undergo electrophilic aromatic substitution. The rate of reaction depends on the…

Q: 7. Which substituent would be classified as a deactivating ortho/para director in an electrophilic…

A: In electrophilic aromatic substitution:Electron donating groups (EDG) are activating and ortho/para…

Q: Draw and name the product(s) and starting material of the following SN2 reaction. Include all…

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Q: Draw the product of an SN2 reaction shown below. Include all lone pairs. Use wedge and dash bonds to…

A: SN2 (Substitution Nucleophilic bimolecular) is a bimolecular reaction. It means reaction take place…

Q: Draw the products of the SN1 reaction below and use wedge-and-dash bonds to indicate the…

A: The given reaction is shown below.We have to draw the products of the given SN1 reaction.

Q: Draw and name the product(s) and starting material of the following SN1 reaction. Include all…

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Q: 1) CH;CH2M9B 2) H20

A: Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: predict the major product and indicate stereochemistry.

A: Reaction of alcohol with PBr3 produce alkyl bromide

Q: а) 1) CH3CH,MgBr 2) H20 b) 1) NaCN 2) H2O

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Q: 4. For each reaction, look at all the reagents and conditions, and determine if the reaction will…

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Q: 1) O3 A bicyclic Starting material H. 2) Me,S H

A: Ozonolysis is the reaction where the ozone cleaves the double bond and forms a carbonyl compound.…

Q: Predict the

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Q: For each of the reactions shown below, indicate the mechanisms that you would expect to see, if any,…

A: Reaction of 3-Chloro-1-butene with Methanol, whose product and mechanism is to be determined.

Q: Please show reaekson and don't use hend raiting

A: The alkyne 2,2-dimethylhex-3-yne undergoes protonation by sulfuric acid.Water adds to the protonated…

Q: Compound A on ozonolysis yields the two products shown. What is the structure of compound A? OOOO OI…

A: we have to determine the structure of compound A

Q: iii) iv) v) Br₂ EtOH Br2 0 °C Br₂, 1 eq

A: The question is based on organic reactions.      we need to identify the product formed and explain…

Q: Predict the major product of the following transformation: A) C) .CO₂Et H₂O* Heat COET C₁0H 100 B)…

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Q: Но….. HO ОН HCI

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Q: Draw the major product formed for each reaction given below. Pay attention to stereochemistry and…

A: Approach to solving the question:This question requires predicting the major products of two…

Q: Which compound shown below would undergo nucleophilic substitution via addition/elimination the most…

A: Given : structure of molecules Tip : more delta positive charge on carbonyl carbon more will be the…

Q: Draw the product(s) of the following reaction, including all stereoisomers: NBS, A peroxide

A: Step 1:Bromination of an alkene by N-bromosuccinimide (NBS) in the presence of light or peroxide is…

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.