Q: stion 11 of 11 Draw the most stable form of the major mixed Claisen product formed in the reaction.…
A:
Q: Be sure to answer all parts. Predict the product and draw a stepwise mechanism for the following…
A: For the above conversion use unimolecular substitution reaction.
Q: Rank the relative rates of the alkyl halides in an SN1 reaction. H3C-1 CH3 CH3 CH₂ H₂C Fastest SN 1…
A: SN1 reaction means unimolecular nucleophilic substitution reaction. The reaction proceeds in two…
Q: Identify the best reagents to complete the following reaction. 1. NaOH А 2. CH3CH2CH2NH2 1. НСІ 2.…
A:
Q: 1. (CH3CH2)2CuLi 2. H3O* 3. LDA 4. CICH,CHCH2 ??? 5. ВНз-THF 6. H2O2, NAOH, H2O
A:
Q: Provide the missing products in the reaction sequence shown below. You need to show the molecule…
A:
Q: 1. На0, кон 2. Н,О, НС он HO, HO. p-cresol chloroacetic acid p-methylphenoxyacetic acid
A:
Q: Complete the following reaction and propose a mechanism.
A:
Q: Provide the ame reaction associated with each reaction below: R-CO-CH3 + N2H/HO" -> Ph-CH2.CH3 Ans…
A: Note: According to our guidelines we are supposed to answer only first three subpart.
Q: 1.68 Provide the missing intermediates and final product in the following synthesis. 1. ВН3 THF 2.…
A:
Q: -78 °C (CH3)3SICI Choose. + (CH2)½CCI ZnCl2
A: Please find the answer attached, here as handwritten note.j
Q: Which of the following is the target product formed after the following sequential reactions? ( ısı…
A:
Q: Be sure to answer all parts. Predict the product and draw a stepwise mechanism for the following…
A: The given reaction will go through SN1 mechanism
Q: COOH COOH OH OH OH OH H3C H3C H3C" Br Select reagents from the table to perform this synthesis; only…
A:
Q: 10. 1. COOH Br 2. 11. OH
A:
Q: H H N H H CL H H
A: Step 1: The strong nucleophile attacks on the electrophile which is alkyl halide. Step 2: leaving…
Q: GS Q1: Show the reactants needed to make the acetal below.
A: Applying concept of deprotactation of alcohol.
Q: Acetal product formation is difficult, since hemiacetals are stable while acetals are not stable.…
A: In this question, we will see this given statement in the Question is true or false. We will…
Q: Step 1 CI Benzoic Acid Thionyl Chloride Benzoyl Chloride Step 2 "y" NH2 HNH Benzoyl Chloride…
A: The process of conversion of benzoic acid into aniline involves the following steps: Step 1:…
Q: This is a multi-step synthesis problem. What reagents are need to carry out the shown chemical…
A: In the above reaction, the Br is being replaced by the ethyl group.
Q: In the following reaction sequence, draw the intermediate formed after the first two steps, then…
A: The reaction shows the intermediate formation with mechanisms - Step 1 -
Q: at would be the major product in the following reaction? Cl2 -CH,CH,CH3 400 °C ect one: a. -CH;CHCH3…
A:
Q: Question 1 Consider the following reaction scheme and answer the questions that follow: || i. CH;CH…
A:
Q: Classify each solvent as protic or aprotic.a. (CH3)2CHOHb. CH3NO2c. CH2Cl2d. NH3e. N(CH3)3f. HCONH2
A: Protic solvents are solvents which contains protons bonded with high electronegative oxygen and…
Q: Step 6: Put it all together. Complete the two-step synthesis by selecting the reagents and starting…
A:
Q: Arrange the reactants from fastest to slowest in an S№2 reaction. (CH3)2C(CI)CH3 CH3CH(CI)CH2CH3…
A:
Q: Please give the appropriate reagents FOR 1, 2 AND 3 to complete the following synthesis. 1 2 3.
A: given reaction is by using Corey-house synthesis reaction we can get the product
Q: Select the correct reagents to carry out the following multi-step synthesis. CH3 CH2-Br CH,-OH CHO…
A: 1. Fridel craft alkylation is electrophilic aromatic substitution reaction in which benzene acts as…
Q: Complete the synthesis below, including all reagents and intermediate products. You don't have to…
A: The reaction in which cyclic adduct is formed by the combination of two or more unsaturated molecule…
Q: OH OH 7. 8. 9.
A:
Q: In each reaction box, place the best reagent and conditions from the list below. There is more than…
A: PCC is very helpful to oxidize a secondary alcohol to ketone.
Q: In each reaction box, place the best reagent and conditions from the list below. 3-Hexanone should…
A:
Q: fill in the product. which crown ether would be best to use in the following reaction to help the…
A: To dissolve the starting material, 18-Crown-6 with a molecular formula of C12H24O6 will be the best.
Q: Match each reaction/phrase with the correct product/answer. v Isobutyl alcohol and warm, basic KMNO4…
A:
Q: Given the follówing proposed mechar reaction. 2A+ 2B C+2D step 1: 2A+B-C+E(slow) step 2: E+B-2D…
A: In any given reaction, slowest step is the rate determining step that means rate of reaction depends…
Q: Arrange the given alcohols in order of reactivity in an acid catalyzed dehydration reaction. O Hold…
A:
Q: Rank the carbonyl-containing compounds in order of susceptibility to nucleophilic attack from most…
A:
Q: 1-bromobutane and Na* OH (SN2 mechanism) 2. 3-chloropentane and K* OC(CH3)3 (E2 mechanism) 3.…
A: The reactions given are,
Q: on он 1. НаО, кон 2. H,O, HCI он, + HO, p-cresol chloroacetic acid p-methylphenoxyacetic acid
A:
Q: 2. Give a stepwise mechanism for each reaction (i) OH 1) CH;MgBr (excess) 2) H2О (ii) OCH3 „NO2 N-…
A:
Q: Propose a mechanism for each of the following reaction: CH3 H20 Br но CH3
A: In this reaction mechanism step first formation of carbocation step second in the ring opening and…
Q: Draw the major product of the given alcohol dehydration in the presence of H, SO4. Use the Zaitsev…
A: Dehydration of alcohol gives alkene as the final product. The transition state is alkene like.…
Q: A set of three nucleophilic displacement reactions is shown below: CH3 CH3 CH3Br CH;CHCH2CH2B1…
A: The correct answer about SN2 reaction is given below
Q: 3. Identify the products (A-G) of each reaction sequence shown below E OH 1) HCI 2) KCN Br NaOCH 3,…
A:
Q: Write the structure of each product/reagent denoted by letters A-F in the foll i) NaOH `NH i) ii)…
A: We will write the final product
Q: What is the rate law implied by the mechanism given below? CH3COCH3(aq) + H+(aq) ←→…
A: The rate law is a mathematical expression that relates concentration of reactants and the rate of a…
Q: Devise a 2-step synthesis of the product from the starting material. CH3 CH3 1. reagent 1 2. reagent…
A: Before solving this question we must know the following reagents _. C6H5CO3H in CH2CL2 =>…
Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr Br ОН OH Part…
A:
Q: 3. Show a mechanism for the following reaction. 8-x-8 OH NO₂
A: Answer : General Reactions : The 2-chloro-5-methylphenol and 3 fluoro-6-nitroanisole to formed…
Which of the following alcohol/s would react to Lucas reagent after:
-
<6 min
-
1-5 min
-
<1 min
Step by step
Solved in 3 steps with 2 images
- A mixture of 0.10 mol benzene and 0.10 mol p-xylene was allowed to react with 0.10 mol nitronium ion until all the nitronium ion was gone. Two products were obtained: 0.002 mol of one and 0.098 mol of the other. a. What was the major product? b. Why was more of one product obtained than of the other?Give the major organic product(s) for each step of the following reactions (d,e,f)(a) Illustrate the following name reactions giving suitable example in each case :(i) Clemmensen reduction (ii) Hell-Volhard-Zelinsky reaction(b) How are the following conversions carried out?(i) Ethylcyanide to ethanoic acid (ii) Butan-l-ol to butanoic acid(iii) Benzoic acid to m-bromobenzoic acid
- II. Alcohols in Synthesis B.) How are alcohols used to make ethers in the Williamson ether synthesis? How do you design the synthesis of ethers using both acidic and basic Williamson ether synthesis strategies?Give the major organic product of each reaction of γ‑valerolactone with each of the given six reagents under the conditions indicated. Do not draw any byproducts formed. Reagent 1. NaOH, H2O, heat, then H+, H2O 2. (CH3)2CHCH2CH2OH (excess), H+ 3. (CH3CH2)2NH and heat 4. CH3MgI (excess), ether, then H+/H2O 5. LiAlH4, ether, then H+/H2O 6. DIBAL, toluene, low temperature, then H+/H2OWhich compound is not a possible product in the reaction below ( F2 is in excess F2and UV light the catalyst).CHA + F2 -->O CFAO CHFaO CHF-O CH2F2O CHaF
- -Reactions E1 and E2 with AlcoholsIt develops the following reaction mechanisms and the main and secondary products:Draw the major organic product you would expect to isolate from the reaction of p-bromoethoxybenzene with a misture of HNO3HNO3 and H2SO4H2SO4.Give the major organic product(s) that would be expected on reaction of 3-pentanone (shown right) with 1 equivalent of LDA, followed by addition of 1 equivalent of each of the following reagents.
- Nitrating methyl benzoate. 1.Describe the mechanism of EAS clearly and in detail 2. What is the effect of subtituent of the outcome of EAS;include 3 classes of subtituentsDescribe how the product is purified. 4,4'-DIBROMOBIPHENYL [Biphenyl, 4,4'-dibromo-] Submitted by Robert E. Buckles and Norris G. Wheeler1. Checked by R. S. Schreiber, Wm. Bradley Reid, Jr., and Robert W. Jackson. 1. Procedure In a 15-cm. evaporating dish is placed 15.4 g. (0.10 mole) of finely powdered biphenyl (Note 1). The dish is set on a porcelain rack in a 30-cm. desiccator with a 10-cm. evaporating dish under the rack containing 39 g. (12 ml., 0.24 mole) of bromine. The desiccator is closed, but a very small opening is provided for the escape of hydrogen bromide (Note 2). The biphenyl is left in contact with the bromine vapor for 8 hours (or overnight). The orange solid is then removed from the desiccator and allowed to stand in the air under a hood for at least 4 hours (Note 3). At this point, the product weighs about 30 g. and has a melting point in the neighborhood of 152°. The crude 4,4'-dibromobiphenyl is dissolved in 75 ml. of benzene, filtered, and cooled to 15°. The…I need specific description of the compounds involved in the synthesis (functional groups, specific features). and also describe the steps involved in the synthesis and the role of each step. And most important!!devote one to each step of the synthesis. Each step should clearly indicate the reagent used, the stereochemistry involved in the reaction and its importance or relevance to the multistep synthesis