5. Show the major product of the following reaction. Justify your answer. OCH EISH H*

Q: Predict the main product of the reaction in Figure 10.

A: Alkyl bromide reacts with ammonia, a nucleophile to give a nucleophilic substitution reaction to…

Q: In order to complete the synthesis shown below, you would need to use [ Select ] as the nucleophile…

A: SN1 reactions are favoured by the attack of nucleophile from the same direction as that of the…

Q: 2) Write a detailed mechanism for the following reaction: он H30* OH

A: we have given that acid catalyzed epoxide opening to give diols.  the details mechanism of reaction…

Q: NO2 Br

A: The conversion is given below in pic.

Q: What is the main product from the reaction sequence below?

A: First, let's discuss the given reaction. The initial reactant used in the reaction is styrene. The…

Q: Complete the multi-step synthesis below by filling in the missing reagents in boxes (a) through (g).…

A: The organic reactions usually involve either substitution reaction, elimination reaction, or…

Q: OH Br

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

Q: Explain why order of operations in this synthesis is important. What product would you form instead…

A: HNO3, H2SO4 is nitrating mixture (adds -NO2 on benzene)  Br2, FeBr3 (adds -Br atom on benzene ring)…

Q: What is the major product of the reaction shown below?

A: Answer: (D)  Nucleophilic addition takes place at aldehyde carbonyl carbon. Nucleophile is alcohol…

Q: Give the major product of the following reaction. MeO H2

A: Given,

Q: What is the product of the below reaction?

A: This is a reaction where the alkynes are getting reduced to trans alkenes in the presence of Na,…

Q: 2. Write the synthetic procedure for the target compound with your own idea. (At least more than 5…

A:

Q: please provide synthesis starting from benzene, use the least amount of steps possible. OCH3 N. CB 3

A: Benzene can be converted to the given compound as follows: Firstly, benzene is treated with Lewis…

Q: propose a synthetic route to this structure that includes at least one C-C bond formation step.

A: 2 -Methylbutanoyl chloride can be synthesized as given below.

Q: 5. Propose an efficient synthesis for the reaction below: OH

A: In this given reaction, the reactant is 3-oxo-methylbutanoate and the product is…

Q: Provide the mechanism for the 5th and final reaction in this synthesis: OH KMAO4

A: This is an oxidation reaction.  Here secondary alcohol is converyed into ketone using potassium…

Q: 3) write a detailed mechanism for the following reaction: Br hv light + HBr + Br2

A:

Q: Show the reaction mechanism for the formation of: a. RCONH2 from the reaction of RCOOR’ with NH3

A: given find mechanism of RCONH2 from the reaction of RCOOR’ with NH3

Q: What is the result of the reaction shown below?

A: The above reaction is the SN2 reaction. here Cl- act as a nucleophile and attacks from the backside…

Q: Show the synthesis for the following Reactions. M Ô olt Nit2 Br -NH₂

A: Please find the attachment

Q: 2. Show the complete mechanism for the following transformation H*, H20

A: The reaction taking place is given as,

Q: 2) Write a detailed mechanism for the following reaction: H2SO4 CH;CH,C=CH + H2O CH;CH,CCH3

A: Hydration reaction of Alkyne takes place in acidic medium as follows:

Q: Which is the major product of the reaction below?

A:

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: 3. For the following synthetic schemes, please draw the product(s) to the right of the arrow. 1.…

A:

Q: CH3OH, H*

A: Aldehyde react with alcohol to give hemiacetal when react with 1 equivalent.

Q: Which compound is a major product of the reaction sequence shown in the box? 1. EtO Na+ OEt 2. HСI,…

A:

Q: 2. Starting from 1-propyne as your sole carbon source for the product, provide the steps required…

A: prop-1-yne undergo reduction with No/Lig NEB to give propens which undergo addition reaction to…

Q: HONH, CI- , NaOH

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

Q: OH OH a) CH3 b) c) Br

A:

Q: Na NH3() diene

A: Reaction of alkynes with Na/NH3 produces alkene. This reaction is stereospecific and gives only the…

Q: NaOCH3 HOCH3

A:

Q: H;O*

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

Q: Ph Na Oet Eto OEt

A:

Q: From the two synthetic routes shown below which one would be the best route for the desired product.…

A: 1) the reaction of cyclohexane react with NaBH4 to give cyclohexanol. because the NaBH4 is reducing…

Q: 3. Please provide a complete step-wise synthesis of the target molecule showing all steps, reagents…

A: 3. Given reaction,

Q: 1. Mg(0) 2. CO2 Br 3. H3O* 1. Mg(0) 2. CO2 3. H3O* Br MeO 1. (CH3)2CuLi 2. H20

A:

Q: Perform a retrosynthetic analysis by working backwards two steps in the synthesis below. Identify…

A: Given  target molecule is alkyl halide.

Q: Please help in predicting the major product of this reaction! Thank you

A:

Q: 2) How do you perform the following reaction?

A: Stork enamine Reaction: Cyclohexanone and pyrrolidine react with each other in the presence of…

Q: CH3 CH3 Br FeBr3. HBr (а) Br2 ČH3 CH3

A:

Q: 5) Show the complete mechanism for an E2 reaction with 1-bromo-2-tert-butylcyclohexane

A: Answer - 1-bromo-2-tert-butylcyclohexane - A chemical structure of a molecule includes the…

Q: 2. Answer ALL parts. a) Write a detailed reaction mechanism for the following conversion. ОН HO…

A: We have to give the mechanism of the given reaction.

Q: (10) Please find out the most reactive substrate in Sn2 nucleophilic substitution. А. CH3 Br В. С.…

A:

Q: Provide the mechanism for the 2nd reaction in this synthesis: D2S04 PSO4

A:

Q: CH3 .CH3 Br H. H.

A: Alkyl halide gives elimination reactions when they react with a strong base. The E2 elimination…

Q: 5. Please write out the mechanism for the following reaction (Note: SN1) CH3OH CH3 Br OCH3

A: Here in this reaction we can see that the nucleophile is not naked nucleophile , so the reaction…

Q: Propose a mechanism for the following reaction (remember to use curved arrows to show the movement…

A: Please go through the below pic for the mechanism.

Q: 1. Excess LIAIH4 MeO НО 2. H2о

A: Given reaction: We have to write the mechanism of the reaction.