Draw detailed mechanisms for the following transformations Мео. Br2, NaOH Meo, NH2 `NH2 H20

Q: H2O H2SO4

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Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: 1)…

A: LiAlH4 acts as reducing agent.

Q: please explain the reaction with mechanism

A: in the given question, it is secondary alkyl halide which reacts with a very good nucleophile. This…

Q: Mechanism 1. Provide the complete mechanism for the reactions below. You must include appropriate…

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Q: OCH3 OCH3 OCH3 Rof [Ca

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Q: 46. Which mechanism(s) would be favored under the following reaction conditions? -CI NaBr DMSO A)…

A: The substrate is a haloalkane and NaBr salt can dissociate to form Br- ion. This Br- can act as…

Q: Provide a complete, detailed mechanism for the reaction CH;CH,OH shown here.

A: A complete and detailed mechanism for the given reaction can be provided as

Q: 5,5-dimethylhept-3-ene was reacted with HBr. Provide the reaction mechanism of this reaction.

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Q: Can you do it and explain it in detail? Show the mechanism

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Q: Please show me the mechanism on paper that way it's easy for me to understand

A: To give the mechanism of the two step given reaction.

Q: What is the mechanism for the reaction?

A: The reaction will have the below mechanism for step 1

Q: OH HO CH3 HC1

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Q: Suggest a synthesis of ketone 6 from (E)-3,4-(dimethoxy)cinnamic acid 9. You can assume that any…

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Q: CCHCH3 CH30 H3CH2C е. CH2CH3 CH3OH

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Q: НО. H3O+

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

Q: Br CH;OK a) b) Sn1 Sn2 c) d) E1 E2

A: Generally, alkyl halide or alcohols undergo elimination reaction which give rise to alkene.…

Q: Can you show the mechanism and explain the steps

A: Dehydration of alcohol in the presence of acid leads to the formation of an alkene.

Q: HBr peroxide

A: To draw the product of the given organic reaction mechanism.

Q: For the following reaction show a reasonable mechanism for the formation of the product

A: In this question, we will write a reasonable mechanism for the formation of the product from the…

Q: C. BLAM Basic Acid-mort H₂SO4 H₂O Epoxide

A: The reaction is an example of deprotection of ketone in an acidic medium.

Q: Confused on how to continue with this mechanism reaction

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Q: Synthesize the following compounds from 4 carbon or less mono-functional alcohols, benzene, toluene…

A: This is Chlorination and bromination reactions. if we take benzene, chlorination of benzene will…

Q: Draw the product of this nydrogenation reaction. Use wedge and dash bonds to indicate…

A: Interpretation: We have to determine the product for the following given reaction.

Q: i) PhMgBr ii) H2O

A: The Grignard reagent is denoted as R-MgX, where R can be an alkyl or aryl group and X is a halogen.…

Q: Predict the major c Select Draw 1. NaOEt/E1OH 2. E1OCOCH,Br 3. dilute NaOH, heat 4. H30* 5. Heat но

A: Active methylene compounds are very acidic proton. Active methylene compounds have two acidic…

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: 1)…

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Q: can someone complete the following mechanism with all steps?

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Q: CH3 CH;=CH(CH2)2 , 'N' 35-47% ČO,H

A: In this question, we will write the mechanism so first we need to redraw the starting material in…

Q: Predict the major organic product of this reaction and draw the complete mechanism to form it: HO-…

A: This reaction generates cyclic anhydride from Dicarboxylic acid by heating.

Q: 17. Explain what is wrong with the following mechanism step and provide an alternative way in which…

A: The reaction step given is,

Q: Which reagents would best accomplish this transformation? %3D .C. HO, CH3 CH3 CH3 (A) K,Cr,O, +…

A: The reaction given is,

Q: 1. Using the two alcohols on the left and any reagents that you need, provide a high yielding…

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Q: H+, H2O

A: Given,the reaction is:

Q: Can someone please explain to me the reaction mechanism of this reaction? Please answer fully and…

A: Please see the attached files.Explanation:Thank You.

Q: 요 NaOCH 3 CH3OH

A: Intramolecular reaction

Q: 7 HW7 - Due: 2/2/2023 8:00 8

A: The given reactions are: 1) 2)

Q: One frequently used method for preparing methyl esters is by reaction of carboxylic acids with…

A: Interpretation -  According to given reaction we have to basically explain the mechanism here -  To…

Q: SN1 Br + H20 -ОН + НВr SN1 Br + H20 -ОН + HBr

A: In SN1 reaction, 1st step is dissociation of the leaving group and form carbocation.  Then…

Q: 23.6 Intramolecular Aldol Reactions Treatment of certain dicarbonyl compounds with base produces…

A: Given reaction is aldol reaction and it is intramolecular aldol reaction. In presence of base first…

Q: Drow thise reaction mechanism

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Q: Can you show the mechanism for those reactions

A: I have solved 4 .  Pls repost your remaining questions seperately.  Thanks

Q: OEt 1. EtO¯Na* `OEt 2. Н.О, НСІ (excess)

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Q: 1.NaH/MDSO/CH3I 2.HNO3/H,SO4 3.Fe/HCI CH3 H3C 'N' NH 4.1.HCCOH/Heat 2.HNO/H2SO4 'N' N.…

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Q: olve correctly please. Can someone draw out the mechanism for this reaction

A: In this reaction conversion of acyl chloride into tertiary alcohol by attack of two moles of gilman…

Q: Can you show the mechanism and do you any rules that will allow you to determine the answer without…

A: The given reaction is the mechanism for the oxidation of primary(1o) alcohol by the strong oxidizing…

Q: tautomerization HO-

A: Given : We have to draw the keto-enol tatutomerization product.

Q: 40. Consider the following reaction: H* + + H;02 - H20 + HOI A student proposes the following…

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Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.