Q: What is the major product of this reaction? 1) LDA, cold 2) CH,Br OH
A:
Q: H3C H + CH3OH (+ excess CH3OH, H+) →
A:
Q: What is the major organic product? 1) EILI (excess) Et20 2) H20 C OH но
A: EtLi is a type of organolithium compound. Where, the organo part is an alkyl group , R (Here, R=Et).…
Q: What is the major organic product obtained from the following reaction? (CH,)2CuLi
A: Haloalkanes and Haloalkenes react with Lithium dimethylcuprate, (CH3)2CuLi ( Gillman's reagent)…
Q: Give the major product of the following reaction. Cl2 (1 mole) CI FeCl3
A:
Q: What is the major product of the following reaction. 1 bromopropane, 1. LiAIH4, 2.H2O.
A: Organic reactions are those in which organic reactant react to form organic products.
Q: What is the major organic product of the following reaction? 1. O3, -73C ECH-CH3 2. Zn, H20
A: The reaction given is,
Q: CHCH3 1. Hg(OAc)2, H20 2. NaBH4 CH3
A: When alkene proceeds through mercuration demercuration process, then OH group attached with least…
Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. Hg(OAc)2, H20 2. NaBH4,…
A:
Q: What is the major product produced in the given reaction? А 1. B C D 4. 1. LIAIH, , ether major…
A: This is the question of reaction mechanism
Q: What is the product of this reaction? 1) Hg(OAc)2, H2O 2. NaBH4 A. он В. C. D. OH
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Q: 5. Which is the major product of this reaction? а. b. C. d. KMNO4, H20 .COOH .COOH Сно HO, НООС
A: Concept : Alkyl side chains of benzene ring can be oxidized to -COOH group by strong reagents like…
Q: Indicate the major organic product from the reaction shown. 1. Li 2. B(OCH3)3 Br 3. Pd(PPH3)4 NaOH…
A: This is an example of cross coupling reaction. It involves four steps. A. Oxidative addition. B.…
Q: The Jones oxidation reaction has two basic parts: addition of chromic acid onto the alcohol (step 1)…
A:
Q: COOH So3. H,SO, CN Cl,, FeCl3 5.
A: A mixture of SO3 ( sulfur trioxide ) and H2SO4 (sulfuric acid ) is called fuming sulfuric acid .…
Q: Draw the major product of this reaction. Ignore inorganic byproducts. 1. Hg(OAc)2, H20 2. NABH4,…
A: Interpretation: We have to draw the major product for the following reaction.
Q: CH,CH, NH, H,C. Br Br NaBH, Br2 FeBr, agua
A:
Q: What is the major product of the following Grignard reaction? OH Он он он OH 1. Mg, THF Br 2. O. CH3…
A: The correct option is (a) The mechanism is as:-
Q: What is the major organic product obtained from the following reaction? OCH,CH, 1. NaOCH,CH, CH,CH…
A:
Q: OH H2SO4 (a) Heat .CI 1.AICI3. (b) + 2.H20
A: Both reactions are possible. Please find the attachment for the solution.
Q: Draw the structure of the major organic product of the reaction. 1. LIAIH4, ether .CI 2. H,0
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Q: What is the product of this reaction sequence? В. OH OH 1. НО 2. LIAIH 3. H2O, H, heat С. D. OH, H*…
A:
Q: Br [(CH3)3C]2CULI
A: To find the product of: (a) (b)
Q: Name the Product for the following reaction: PBR3, ether ? OH
A: This is the reaction of converting alcohols into alkyl halides. this reaction will undergo by SN2…
Q: Draw the organic products formed in each reaction. [1] NaH (2) Br (1] NANH, [2]
A: The reactions given are,
Q: What is the product using these reagents? 1) Mg, Et2O; 2) D2O.
A: The Answer to the following question is-
Q: Write the structural formula of the organic product for the given reaction between an alkyne and an…
A: Given reaction is alkylation reaction of alkyne.
Q: 1) BH3, THF 2) H2O2 H,O, NAOH 10. 3) NaH 4) CH3B
A:
Q: What is the major organic product obtained from the following reaction? HO, HO 2 PCC HO, CH2CI2 но.…
A: Given reaction,
Q: Draw the major organic product for the reaction below. Br 1) PPH3 2) n-butyllithium 3) O Н
A: The given compound is bromocyclopentane as shown below:
Q: Draw the structure of the major organic product(s) of the reaction. H30 N-
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Q: Oxidize the below molecule as many times as possible. Then name each product. Br OH…
A:
Q: ОН H2SO4 (а) + Нeat .CI 1.AICI3. (b) 2.H20 (0)
A:
Q: Explain why two substitution products are formed in the following reaction.
A: Nucleophilic substitution reaction is a two-step reaction. A nucleophile is substituted at the…
Q: Ques- what is the product of the following reaction? CH₂- that рад ether эх у OH (A) 0 € 04 B D D OH…
A:
Q: What is the major product of this reaction? 1) NaOEI 2) H*
A: Ester: Esters are the organic compound having general formula of RCOOR'. It is derived from acid in…
Q: Give the major product for the reaction. OH, Heat
A: In the given reaction, at first OH- will abstract a proton. Then the anionic end will attack at the…
Q: In each of the following reactions, two possible organic products can be formed. Draw both organic…
A: 1,2 or 1,4-addition depends on mostly by the nature of the nucleophile. There is a competition…
Q: Draw the major product of this reaction. Ignore inorganic byproducts and COM. 1. KMNO4, OH- (warm)…
A:
Q: 4. What are the products obtained from the following elimination reaction? Indicate the major…
A: “Since you have asked multiple question, we will solve the first question for you. If you want any…
Q: Dilute H„SO, HBr 2.
A: Note: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question…
Q: What is the organic product obtained from the following reaction? CH,CO,H CH3 CH3 H3C H3C H3C CH H3C…
A: When alkene is treated with per acid then we get epoxy Compound.
Q: #2504 5. Based on what you know regarding the oxidation of primary, secondary, and tertiary…
A: As per the guidelines, I am allowed to answer one question at a time. Please repost the rest. Sorry…
Q: Select the structure of the major product formed from the following reaction. H30* HO, он HO, OH
A:
Q: 1. ВНя/THF 2. H2О2/NaOH
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Q: Cけ3CH2 Cミく Mat BrCHa CH, CH CHa OH
A: Given,
Q: 8. Draw the structure of the product of the reaction displayed. 1) ВН:THF 2) H2O2, OH
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Q: What is the major organic product obtained from the following reaction? 2 mol Br2
A: In this reaction , an alkyne is given and reagent given is Br2 . Br2 ia a reagent which add at…
Q: What is the organic product formed in the following reaction? H', Hg*2 CH,CH,CH,C=CH + H,O I II II H…
A: Electrophilic addition reaction is an addition reaction in which reactant is initially attacked by…
Q: Determine the products of the following oxidation reactions 1. 1-pentanol + K2Cr2O7 =…
A: 1) 1-pentanol + K2Cr2O7 1-pentanol is oxidized to aldehyde in the presence of K2Cr2O7 which is…
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- Why do we have to cool the test tube to 100oC before we add the ethanol. The melting point of the product is 258oC. Why should we not do a mp of the product? The intermediate in brackets loses CO to form the product at 180oC. If the C=O were replaced by CH2, do you think the same type of reaction would happen with loss of :CH2?#1. Part A. in a drug discovery program, a hit compound________. A. Shows activity in an animal model of disease B. Is active in target/ whole-cell assays in vitro C. Is purchased from a commercial vendor D. Is derived from screening natural product libraries Part B. When using TLC to monitor an organic chemistry reaction, which could be an indication that your desired reaction has gone to completion? A. the stationary phase changes colors B.the mobile phase runs to the top of the tlc plate C.the starting material spot disappears and a new spot appears D,the starting material spot remains on the tlc plate. Highlight all the safety features mentioned. Is this reaction more dangerous than most reactions? 4,4'-DIBROMOBIPHENYL Robert E. Buckles and Norris G. Wheeler1. 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 resulting crystals are filtered, giving a…
- Hi! can anyone here help me to create a schematic diagram about the experiments: " 21. Preparation of Ethyne" by Pdst Chemistry, and "Activity 10: Functional Group Tests for Hydrocarbons" by FRETZ RMT since i dont know what a schematic diagram is, and what processes/contents should be in it. thank youWhat is the main organic product (B) of the reaction scheme in Figure 11? [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html. Copy the notation (CTRL+C) and paste it as the answer to this question (CTRL+V).] * Your answerOrganic Chem. This CANNOT be hand-drawn, explanation and illustrations must be typed or digital. if it is hand-drawn your answer will be incomplete and marked as wrong. Molecule: Benzocaine Please describe in a paragraph why 100% ethanol is required as a solvent and why 95% ethanol would not suffice. Any applicable theory or principle should be clearly stated and explained. The balanced chemical reaction and mechanism might prove helpful in answering this question.
- Calculate the % yield-show work in a clear organized matter-be aware of significant figures. Which is the limiting reagent? A Freidel – Crafts Alkylation Name_______________ Data: Alkyl chloride used________tert-butyl chloride___________________________________ Mass alkyl chloride____15.7549 g_______________________________________ Mass 1,4-dimethoxybenzene_____5.0035 g_______________________________ Mass product isolated____2.7834 g______________________________________ Appearance of product__________dry snow white solid________________________________ m.p. rextal product__101 deg Celsius ____________________________________________ Published m.p. product____102-104 o C_____________ source____Chemspider________________ Name of product__1,4-di-tert-butyl-2,5-dimethoxybenzene._______________________________________________Provide details about the reaction workup. 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°.…Using the data below calculate the percent yield for the formation of the ether product in the acid catalyzed condensation synthesis of Methyl beta Naphthyl ether? Weight of 2-napthol ____0.505g_______________ Volume of methanol ____2ml______________ Volume of concentrated sulfuric acid _________1.0ml________ Weight of crude product ____0.295g__________ Weight of purified product ___0.144g_________ M.P. Of Product (If solid otherwise write Liquid) _____70-75 C___________
- In parts 1 and 2 draw the two organic products of this reaction, showing any nonzero formal charges. Then, in part 3 answer the question regarding purification of the reaction mixture. 1. Draw the product with the higher molecular weight here 2. Draw the product with the lower molecular weight here 3. Which method would be the simplest and most effective means to best separate the two products? (extraction, recrystallization, chromatography, distillation)What is the main product of the reaction in Figure 6? [Generate a SMILES notation: https://jsme-editor.github.io/dist/JSME_test.html.Draw the oxidation reaction. Be sure to label initiation, propogation, and termination of free radicals. 150 uL Benzyl Alcohol + 2 mL chlorobenzene + 700 mg N-iodosuccinimide Allow reaction to mix for 90 minutes with a sunlamp.