Q: What is the major product of this reaction sequence? О в ден H LDA THE 0 OH H2O OH 0 H OH OH о- H
A:
Q: Which of the reactions shown below are correct? 0 O HCI H₂O + (CH3)NH + CH3NH2- CHO NHITCH a + H₂O…
A: When an aldehyde reacts with an amine, the product formed is an imine. The imine can be converted…
Q: III. Propose a synthetic route with the least number of steps. possible to carry out the following…
A:
Q: Draw the major product of this SN1 reaction. Ignore any inorganic byproducts. CH3OH OTS a
A: Substitution reaction is an organic reaction where a functional group is replaced or substituted by…
Q: 1) Provide an explanation for why the syn-product shown is favored in the following reduction…
A: Smaller nucleophile will always attacks from the axial direction do the H will be below the plane…
Q: Draw the product of the reaction shown below. Ignore inorganic byproducts. NaBH 4
A: Given reactant is aldehyde. Reagent is NaBH4 , MeOH .NaBH4 is mild reducing agent it reduces…
Q: Predict the stereochemistry of the product for the reaction shown below, clearly illustrating the…
A: This reaction is called Corey-Bakshi-Shibata (CBS) reduction.
Q: Give detailed mechanism Solution with explanation needed. Don't give Handwritten answer..don't copy…
A: pSSteppSStep It is an example of E2 elimination reaction where base takes up the proton which…
Q: Which of the following is the major product of the reaction shown? OH and 01 Oll dilute H₂SO4 سلم لي…
A: In the given reaction first H2SO4 gives hydrogen to carbon carbon double bond to form a carbon…
Q: Provide the major organic product in the reaction shown below. 1. SOCI₂ OH 2. CH3CH2CO₂Na
A: Find out product of reaction.SOCl2 act as Chlorinating agent
Q: Indicate, by letter(s), the position(s) on the ring at which substitution occurs when the aromatic…
A: When simple benzene is treated with Br2 in the presence of FeBr3 (Lewis acid) undergoes…
Q: How many 율 ㅇㅇㅇㅇ STION 4 H₂C 1 2 3 4 CH3 of the starting materials below can be used to complete the…
A:
Q: Mechanism. Provide the complete mechanism for the reaction below. You must include appropriate…
A:
Q: What is the major organic product obtained from the following sequence of reactions? LOH TaCl NaBr…
A: Alcohol can be converted into an ether by a nucleophilic substitution reaction mechanism. In the…
Q: Write the major organic products of the following sequences of reactions. Refer to your reaction…
A: 1. KOtBu:When an alkyl halide reacts with t-BuOK (tert-butoxide potassium), it undergoes a…
Q: Choose the best option for the immediate precursor to this S A HS Br B H
A: The reaction for synthesis of thiolene from the given reactant follows the SN2 pathway. Only HBr…
Q: Propose a complete mechanism and predict the product for the reaction below. Show perspective…
A:
Q: PPh,
A: When triphenyl phosphine reacts with aldehyde molecule, after rearrangement mechanism, it produces…
Q: Draw the major organic product for the reaction below.< 'Br 1) PPh3 2) n-butyllithium 3) H3C CH3
A: The conversion of carbonyl compounds into alkene by the reaction with the triphenyl phosphonium…
Q: CH3 CH3 A) (CH3CH₂)₂CuLi 1. 2. H₂O What is the product formed in the following reaction? Br + B)…
A:
Q: MeO. OH H OMe NO₂ CHO OMe 1. NaBH4 2. PBr3, Py 1. PhOCSC1, Py 2. Bu3SnH, AIBN OSIMe₂t-Bu
A: NaBH4 is one type of reducing agent will reduce all aldehyde, ketone and Iminium ion. Then we use…
Q: None
A: -> NaN3 has nucleophilic part N3- which is a strong nucleophile and give SN2 reaction when reacts…
Q: What is the major product of the following reaction? ८.१ Heat Give detaile. Solution wit needed,…
A:
Q: Give detailed mechanism Solution with explanation needed. don't give Handwritten answer
A:
Q: Show product and provide mechanism NO2 LiAlH4 THF, RT LiAlH4 THF, RT
A: The objective of this question is to write the product and mechanism for the given reaction.
Q: What is the major organic product obtained from the following acid catalyzed hydration reaction?…
A: This reaction goes through carbocation intermediate. Stable carbocation leads to get the major…
Q: Give clear detailed mechanism Solution with explanation needed..don't give Handwritten answer
A: The given reaction is called aldol condensation reaction.On the rectant side aldehyde and ketone…
Q: Give the product of the following reaction: Selected Answer: Answers: B A B None of the above D…
A: Organic reactions are those in which organic reactants react to form organic products. In the given…
Q: B) Provide the MAJOR products for the reactions below and the mechanism for the formation of the…
A: Given are pericyclic reactions. These reactions are known as Diels-Alder reactions.This is [4+2]…
Q: What is the major product of the following reaction?
A: When the benzene reacts with an alkyl halide in the presence of a Lewis acid catalyst alkyl benzene…
Q: Give detailed mechanism Solution with explanation needed..don't give Handwritten answer
A: Dehydration is the removal of water molecules from the alcohol which produces the double bond. This…
Q: NH MgBr K 1. NaOH M 2. CH,CH,Br 1. LIAIH, ether H00 N. 2. CH,OH 2. Но
A:
Q: Give the major product of the following reaction. H₂SO4 H₂O O There is no reaction under these…
A: This is hydration reaction. Alkene react with h2so4 and water to give alcohol
Q: How I can make this product if i start with toluene (explain please ) with mechanism
A: The chemical reaction via which one organic compound converts into other is known as organic…
Q: Design a synthesis of 3-methyl-2-hexene (both E and Z isomers) from ethyl bromide and 2-pentanone.…
A:
Q: What is the product(s) of the following hydration reaction, if any? + H₂O H cat
A: Alkene gives hydration reactions in the presence of an acid catalyst. The reaction follows an…
Q: 5. Draw the products and a mechanism for the following reaction. CO2H H* + CH3CH2OH
A: Esterification: The reaction of carboxylic acid with an alcohol in the presence of acid catalyst…
Q: Draw the major product of this reaction. Ignore inorganic byproducts. Mill POCI3 pyridine Drawing H…
A: Alcohol reacts with POCl3 and pyridine to form an alkene and a phosphate ester.
Q: Draw the major product(s) of the following reaction. CH3 Give detailed mechanism Solution with…
A: This is the addition reaction of olefin,at first protonation occurs at the double bond and form a…
Q: Synthesize the following compounds with any starting materials you'd like (within reason!)!
A: We have to synthesize of 1-phenyl-1-butyne from suitable reactants and reagents.
Q: Determine the major product of each reaction in Problem and draw the complete, detailed mechanism.…
A: Appropriate mechanism and stereochemistry are given below
Q: Draw three organic products of the following reaction. CH₂ + Br₂ FeBr3 Select Draw Templates Br More
A: The aromatic compound reacts with bromine in the presence of a Lewis acid catalyst from bromoarenes.…
Q: Br H3CH₂CO- Na+ ethanol
A: A question based on reaction mechanism. Two reactants that undergoes elimination reaction are given…
Q: Identify the missing reagents / intermediates in both the sequences given below. A ? CN ? -NH R CO2H…
A: In this question, we will Identify all the missing Reagents and Intermidiates. You can see details…
Q: Question is attached
A: Step 1: Conversion of alcohol to aldehyde using mild oxidizing agent, such as PCC. Step 2:…
Q: Propose a synthesis to form cyclohexyl cyclohexanoate using methylene cyclohexane as your only…
A: Given is organic synthesis reaction. The given product is cyclohexyl cyclohexanoate.The given…
Q: Predict the major product for the reaction shown below. TsCl, py ? OH
A: We are given an organic reaction and we have to tell the major product of the reaction.
Q: Which is the best method for carrying out the following two-step transformation (as shown in…
A:
Q: What is the most likely product of the following reaction? _OH DMP CH₂Cl₂ 11 OH
A: DMP is a oxidizing agent and CH2Cl2 is solvent here. The full name of DMP is Dess-Martin periodinane…
please give product and step by step explanation with mechanism of this 2 question
Step by step
Solved in 3 steps with 1 images
- Only one of the chlorine atoms in the molecule, 3,4-dichloronitrobenzene, will undergo nucleophilic substitution. Indicate which position will react and provide the expected product for the given reaction using reaction intermediates (resonance structures).Alcohols are important for organic synthesis, especially in situations involving alkenes. The alcohol might be the desired product, or the OH group might be transformed into another functional group via halogenation, oxidation, or perhaps conversion to a sulfonic ester derivative. Formation of an alcohol from an alkene is particularly powerful because conditions can be chosen to produce either the Markovnikov or non-Markovnikov product from an unsymmetrical alkene. Using your reaction roadmap as a guide, show how to convert 4-methyl-1-pentene into 5-methylhexanenitrile. You must use 4-methyl-1-pentene and sodium cyanide as the source of all carbon atoms in the target molecule. Show all reagents needed and all molecules synthesized along the way.1c. What is the nucleophile in the following reaction? .Br CH;CO0 Na LO OCCH3 NaBr ld. What is the electrophile in the following reaction? Br CH;COO Na L0OCCH3 NaBr +
- The SN2 type reaction will end up with the substitution 2903 the at the reaction center of the reaction. 903 182903 SEY 90374. Predict the products of the following synthetically useful reactions.' NO2 Znº Acetic Acid NH2NH2 KOH heat#16d. Provide the missing reactants, reagents, or products for the following reaction sequences below.
- S.10. Describe the product formed as a result of the reaction between cyclohexanone and 3-butene-2-one by also writing the mechanism of the reaction. 1'CH,ON H;C, 2 HO CH,1. Predict the product, and propose a mechanism for the following nucleophilic addition to aldehyde or ketone. Are the products different from one another? Why do the reactions proceed via different mechanisms? Note the charges on the intermediates of acid and base catalyzed reactions. Oxygen nucleophile in acidic condition H2O, [H+] Oxygen nucleophile in basic condition NaOH5.Synthesis. Make the following products from a suitable cyclic alkene starting material. Look at the functional group PATTERN present in the molecule, including stereochemistry. CH3 ОН ОН CH3