Give the major product of the following reaction 1 naoh 2 ch3ch2ch2cl

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Alkyl Halide to cis-Diol: An alkyl halide can be converted to a cis diol through a series of reactions. An alkyl halide can undergo elimination reaction to give an alkene.

THF 2) H 2 O 2, NaOH H 2 /Pt Br 2 /H 2 O Br 2 NaOMe O-HBr TsCl/pyridine Br Br HBr/H 2 O 2 Klein, Organic Chemistry 1e Answer: L, H, E OR D, K, H, E For more examples of this type of problem, see Skillbuilder 9.10 and 9.12.

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1) Please write the product of the following reactions. 2) Please indicate the starting material required to produce the product. 3) Please draw the structure of the oxaphosphetane which is made during the mechanism of the reaction given that produces product C .

Give a detailed description for reaction mechanism for the reaction expected to occur when 2-bromo-2-methylpentane is heated with sodium methoxide. Draw clear structural formulas of all relevant species and use curved arrows to represent electron flow. Also indicate which step is likely to be rate-determining.

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Give the correct product for the following reaction: a) b) c) COOH COOH d) CHO CHO CH 2 OH CH 3 CH 2 C C CH 3 D 2 Lindlar catalyst C C H 1. BH 3 , THF 2. H 2 O 2 , NaOH, H 2 O KMnO 4 H 3 O + D 3 e) CH 2 OH

3. (15 pts) Fill in either starting materials, reagents or major products for each of the following reactions. Show stereochemistry where relevant. Cl O OH O CO 2 Me 1. NaOEt, CH 3I 2. H 3O +, OH O NaOH, EtOH (2 compounds) NH O LiAlH 4 O O PhMgBr (excess)

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(d) 2-chloro-1-pentene (e) all of the above have a mirror image isomer 8. Which of the following is not a possible product from the reaction of 1-methylcyclohexene with NBS and light? Br Br (a) (b) (c) (d) (e) H3CBr all are possible products CH3 Br 9. 1-Bromocyclohexene can be converted to 1-methylcyclohexene by the reaction with which of the ...

Propan-1-ol undergoes dehydration in the presence of protic acids (such as H 2 SO 4, H 3 PO 4) to give 1-propoxypropane. The mechanism of this reaction involves the following three steps: Step 1: Protonation. Step 2: Nucleophilic attack. Step 3: Deprotonation

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40. What is the product of the following reaction? 41. What product or products are expected from acid-catalyzed hydrolysis of the following compound? (a) only the starting material itself (no reaction) (b) benzaldehyde and 2,2-dimethyl-1,3-propanediol (c) benzoic acid and 2,2-dimethyl-1,3-propanediol (d) 2-phenyl-1,3-propanediol and acetone 42.

If the compound is an alkyl halide, indicate whether it is 1°, 2° or 3°; and also if it is allylic or benzylic. ! Circle any organic halide below that can undergo a S N1 or S N2 type substitution reaction. Cl Cl 1-chloro-2-methylpropane (2R, 3R, 6S)- 2 chloro, 8 ethyl, 3,6 dimethyl decane Cl Br Cl I F Br I Br F alkyl, 1o, SN2 allylic 3o,S N1 ...

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Ans. sol. Ans. sol. For the following reaction. equilibrium constant Kcat 298 K is 1.6 x 1017 (aq) FeS(s) e(aq) When equal volume of 0.06 M Fe+2 and 0.2 M S-2 solution are mixed, then equilibrium concentration of

12. Predict the MAJOR product of the following reaction: 2,3-dimethylcyclohexanol + H 2 SO 4 A) B) C) D) E) Page 9 13. Predict the MAJOR product of the following reaction

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Oct 23, 2018 · In a reaction, the major product would be the product that is most stable and therefore more likely to form. An example would be electrophilic addition of propene with HBr.
The reaction will happen in three steps: 1. The double bond will attack H+ to give a Markonikov product with formation of cation at second carbon atom. 2. There will be a hydride shift from the third carbon to the second one because tertiary carbo...
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Nov 01, 2013 · When 2.50 mol of Mg3N2 are allowed to react according to the following equation, how many moles of H2O also react? Mg3N2 + 6H2O ---> 3Mg(OH)2 + 2NH3 . Chemistry. Consider the following mixture of SO2(g) and O2(g).If SO2(g) and O2(g) react to form SO3(g),draw a representation of the product mixture assuming the reaction goes to completion.
Sep 13, 2020 · 3) Predict the major product of the following reaction. 4) (True or False) – There is no way of controlling the product ratio of E1 / S n 1 reactions. 5) Explain why the presence of a weak base / nucleophile favors E1 reactions over E2.
Jan 22, 2017 · The more stable (major) alkene product is 1-methylcyclohexene and the minor product is 3-methylcyclohexene. d) 2,2-Dimethylcyclohexanol. The initially formed 2° carbocation undergoes a methyl shift to form a more stable 3° carbocation, which loses a proton to form 1,2-dimethylcyclohexane as the major product. The 2° carbocation can rearrange ...
8. (20 pts) Furan (1) undergoes rapid bromination to give 2-bromofuran (2) as the major product as shown.; very little 3-bromofuran (3) is formed. a) Write the mechanism for the bromination of 1 to give 2 showing all proton transfer steps and symbolizing the flow of electrons with curved arrows.
Propan-1-ol undergoes dehydration in the presence of protic acids (such as H 2 SO 4, H 3 PO 4) to give 1-propoxypropane. The mechanism of this reaction involves the following three steps: Step 1: Protonation. Step 2: Nucleophilic attack. Step 3: Deprotonation

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The rate of the reaction, that is, how fast the reactants change over into products depends on the height of the activation barrier NOT the energy difference between reactants and products. Imagine that there are 2 different ways for A to transform into B. Pathway 1 has a high activation barrier (high E act). It requires a great deal of added ...

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A 1, 2, and 3 B Only 1 and 3 C Only 3 D Only 2 E Only 1 BONUS : The reaction of 4-hexen-1-ol with bromine in ether (solvent) gives a compound with the molecular formula C 6 H 11 BrO.

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Jan 18, 2012 · Yes, the temperature greatly affects the product. At low temperatures you will obtain the 1,2-diol (glycol). At higher temperatures the 1,2-diol will cleave and you will get a reaction product essentially equivalent to ozonolysis.

Since, this reaction is given by the compunds with ( CH3 - C0-) group. So, (2) CH3COOCOCH3 and ( 3) CH3CONH2. GIve yellow precipitate by the formation of Iodoform. -2.

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Summary of S N 1, S N 2, E1, and E2 Reactivity. The following chart and table summarize the expected modes of reactivity es, although the reader should recall the alcohols, under acidic conditions, can react in the same ways (except for E2, which requires base).

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The crystallized product is a hydrate, Na 2 SO 4 ·10H 2 O, commonly known as Glauber’s salt. Sodium thiosulfate (sodium hyposulfite), Na 2 S 2 O 3 , is used by photographers to fix developed negatives and prints; it acts by dissolving the part of the silver salts coated onto film which remain unchanged by exposure to light.

45. The following is not an appropriate reaction for the preparation of t-butyl ethyl ether. (i) What would be the major product of this reaction (ii) Write a suitable reaction for the preparation of t-butylethyl ether. C2H5ONa (CH3)3-Cl C2H5-O-C(CH3)3 Ans (i) The major product of the given reaction is 2-methylprop-1-ene.

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Mar 17, 2008 · 1- Butanol 1- bromobutane. step via a Lewis acid-base reaction to give the oxonium ion 1. This oxonium ion then undergoes displacement by the bromide ion to form 1-bromobutane and water. This process is an SN2 reaction in which water is the leaving group and bromide ion is the nucleophile.

Dec 04, 2012 · 2 comments :)-I think it may be important to say that in the truly ‘toss up’ cases (like #2 above), if we ran the reaction and analyzed the results by, say, GC/MS (something we do in our ugrad OChem labs… tho not for this reaction), we’d probably see BOTH E2 and SN2 products… but with protic solvents the E2 is the major organic product, and with aprotic solvents the SN2 is the major ...

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