Predict the product and write the complete stepwise mechanism. for the following reaction. Show all electron flow with arrows and draw the intermediate structures. Then H* + NaSCH3 +

Q: 1. 2. 3. Br NO₂ H₂SO4 Br₂ FeBr3 AICI3

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Q: Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the…

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Q: Show the organic product formed when 4-methylpentanal is heated with sodium methoxide in methanol as…

A: We will find out the reaction product

Q: Complete the following reaction by adding major product. „Br + NAOCH3 CH,OH (solvent) hv • Br2 c)…

A: “Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Complete the following sequence of reactions by indicating the missing reagent(s). Also, show the…

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Q: Consider the E2 elimination of 3-bromopentane with hydroxide. :Br CH3 product + Br+ H2O H CH3CH2…

A: E2 mechanism is a bimolecular elimination method.  It is also known as concerted mechanism because…

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

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Q: Hg2+ Но c=CH2 H3C H3C-C=C-H H30

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Q: 5. Complete the outlined reaction sequence by drawing structures for the major product expected. Yo.…

A: Nitro benzene is meta directing towards electrophilic reaction.

Q: ii) a) Compound 1 reacts with LICKOR superbase ("Buli/"BUOK) to provide carbene 2. The reaction of 2…

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Q: Write the complete and detailed mechanism for THREE EXAMPLES of SN1 reactions. In each example ,…

A: Number of functional group is associated with organic compounds which impart specific chemical and…

Q: Na O H:0 Select to Add Arrows NaH Na O Он H :0:

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Q: and give the major product formed

A: Alkynes undergo addition reaction with electrophiles like halogens. Halogens are attached with the…

Q: Cl2

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Q: H. NH2

A: The reaction taking place is given as,

Q: Write a mechanism for the step shown below, using curved arrows to show electron redistribution.…

A: In acidic medium, oxygen of substrate takes the proton of acid. And if already oxygen is protonated…

Q: ОН H, SO, → product Step 1: Use curved arrows to complete the Step 2: Use a curved arrow to show the…

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Q: 3-) Show the mechanism by using curved arrows for the reaction between following lactone and…

A: Grignard reagent first attacks the C=O of the cyclic lactone through nucleophilic addition reaction…

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

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Q: Show how HC≡CH, CH3CH2Br, and (CH3)2CHCH2CH2Br can be used to prepare CH3CH2C≡CCH2CH2CH(CH3)2. Show…

A: SN2 reaction:  The alcohols is reaction with acids like hydrochloric acid or hydrobromic acid, the…

Q: From Cyclopentane `CO2H CO2H

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Q: Draw the structure of the product for the reaction below. Write the complete stepwise mechanism for…

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Q: Consider the reaction. 1. NaBH, 2. D20 H. Complete the electron-pushing mechanism for the reaction…

A: We have given that the reaction is reduction of benzaldehyde by NaBH4 to give alcohol.

Q: Show the product and arrow pushing mechanism for the following reaction. Make sure that label the…

A: The product of the given organic reaction is as follows.

Q: Na O Select to Add Arrows NaOH Na O H. Br:

A: When atoms combine to make a compound, energy is always given off, and the compound has a lower…

Q: Complete the following S1 reactions by showing the major productis). Pick two and show the complete…

A: Given all are the examples of SN1 reaction mechanism. Firstly a carbocation is formed then the…

Q: H3C CH3 H3C CH3 Br NaH H.

A: Terminal alkynes on reaction with strong base, Sodium hydride (NaH) gives the corresponding…

Q: Show a mechanism for how the product is formed. Your mechanism must use curved arrows to represent…

A: Given : reaction It is an elimination reaction, since strong base is given so it is E2 elimination.

Q: H* OH

A: This is an Esterification Reaction. In this, acid react with alcohols to form ester in presence of…

Q: Select the major organic product of the reaction. NaBH4, MEOH product

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Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: Curved arrows are drawn to indicate the flow of electron from electron rich site to electron…

Q: Predict the product and write the complete stepwise mechar for the following reaction. Show all…

A: The given starting material, epoxide, also called oxirane which is treated with sodium thiomethoixde…

Q: Complete the curved arrow mechanism for this reaction including the charges where necessary CO,Me N…

A: Electrophilic aromatic substitution is an organic reaction in which an atom that is attached to an…

Q: 3) write a detailed mechanism of: HO -OH CH3ČCI AICL3 CCH3

A: The reaction of phenol with acetyl chloride in the presence of anhydrous AlCl3 to form…

Q: Using curved arrows to illustrate the flow of electrons, propose a mechanism to account for the…

A: In this question, we will draw the reaction mechanism by using curved arrows and showing all the…

Q: Show the mechanism for the following transformation HO.

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Q: HONH, CI- , NaOH

A: This is an example of condensation reaction in which hydroxylamine condensed with 1,3-dikketone to…

Q: Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing…

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Q: H;O*

A: In the given reaction the alkene is hydrated to form an alcohol.

Q: Show the retrosynthesis mechanism of this equation with curved arrows representing electron transfer…

A: Note : 1-Butene on hydroboration and oxidation produces the 1-butanol. Benzoic acid and 1-butanol…

Q: In each case below select the synthetic procedure that could be used to carry out the transformation…

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Q: Complete the mechanism for the hydrolysis shown by adding any missing bonds, charges, nonbonding…

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Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

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Q: Show how HC ≡ CH, CH3CH2Br, and (CH3)2CHCH2CHBr can be used to prepare CH3CH2C ≡ CCH2CH2CH(CH3)2.…

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Q: Complete the following nucleophilic substitution reactions. In each reaction, show all electron…

A: The reaction is completed by nucleophilic substitution reaction, where Br- is a leaving group and…

Q: 3-) Show the mechanism by using curved arrows for the reaction between following lactone and…

A: Question a compound of lactone is a reaction of ethyl magnesium bromide and H3O+ can be mechanism is…

Q: H3C Br HBr H3C-C=C-CH3 c=C CH3

A: GIven The reaction involves addition of HBr to symmetrical alkyne. Since the alkyne is symmetrical,…

Q: Show the product of the reaction below, along with a mechanism for its formation. Provide a Newman…

A: LDA is lithium diisopropylamide. It is a strong base. Its structure is, On reaction with alkyl…

Q: What

A: We will write the product

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.