The original alkene can now undergo an alkoxymercuration-demercuration reaction with the alcohol prepared in the first step. Draw the product of the following alkoxymercuration-demercuration reaction. OH 1) Hg(OAc. 2) NaBH,
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Q: он 1. Hg(OAC2, H20 2. NABH,
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A: IUPAC Name=?
Q: OH 1. Hg(OAc)2. H20 2. NABH,
A: Product can be synthesized from the reaction of an alkene with Hg(OAc)2 followed by reduction with…
Q: NO2 2. Starting from only cyclohexane as the sole carbon source, synthesize the ether below.
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Q: 7.55 Acid-catalyzed dehydration of 2,2-dimethyl-1-hexanol gave a number of isomeric alkenes…
A: Acid catalysed dehydration reaction.
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A: The chair form of the above molecule(trans-decalin) can be drawn as follows.
Q: OH 1. Hg(OAc)2, H2O 2. NABH4 .CH3 CH3 H2C H3C Acid-catalyzed addition of water to an alkene yields…
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A: Since you have posted multiple questions, we are entitled to answer the first only.
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Q: 14.47 What alkenes might be formed by dehydration of the following alcohols? If more than one…
A: Organic chemistry: As per our guideline we have to answer first three Sub-questions only.
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- Draw the product of the reaction of 1,2-dimethylcyclohexene with [math]H_{2}[/math] over a Pd catalyst. Show stereochemistry with wedged and dashed bonds.1. Draw 2 neutral product(s) of oxymercuration (Product A). Draw hydrogens bonded to oxygen, where applicable. Clearly show stereochemistry. 2. Draw the alcohol product(s) of demercuration (Product B). Include stereoisomers, if any. 3. Select all the characteristics that apply to the alcohol product(s).96) Which of the following statements is false? Hydroboration-oxidation reaction of alkenes is not complicated by rearrangement of carbocations. Hydroboration-oxidation reaction of alkenes produces alcohol. Hydroboration-oxidation reaction of alkenes produces an anti-markonikov product. None of the above
- Explain the reaction mechanism of the reaction below? (Identify the type of reaction, the species (Nucleophile an electrophile) involve in the reaction after bond cleavage and the IUPAC name of the major product.During the further development of other prostaglandin-like molecules, it is necessary to replace the cyclopentane ring with the cyclohexene as shown in the reaction scheme below. (Deuterium (D) is a heavier isotope of hydrogen) a) Draw the most stable conformation of the starting material 8 and explain why this is the most stable conformation. b) Draw the reaction mechanism for how 9 is formed from 8 and explain why 10 and 11 are not formed if one assumes the E2 mechanism.Consider a reaction where cis-but-2-ene is treated with OsO4 followed by NaHSO3/H2O. Draw the structure of one product that is formed in the reaction, including correct stereochemistry.
- 2-butanol + NOx + hv (assume the carbon-hydrogen bond on the carbon adjacent to the carbonwith the alcohol group is the weakest) For each mechanism, provide the photolytic cycle, a source for hydroxyl radical (if needed) AND atermination step. You may stop when you have accounted for all radicals AND all VOCs are stable (i.e., ifformaldehyde is a product of your mechanism, you do not have to oxidize that molecule to).Draw the major organic product obtained from the reaction of the following alkyl halide with hydrosulfide. Be sure to include the correct stereochemistry.a) Draw both chair conformations of the starting alkyl bromide. Indicate which conformation, if either is more stable. Briefly justify your answer. b) The starting alkyl halide has two chiral carbons. What are the configurations (R/S) at each of these carbons? c) Identify the mechanism (E1/E2) which reactions 1, 2, and 3 proceed by. d) Provide mechanisms that explain the products formed in reactions 1, 2, and 3. All electron movement must be shown in order to receive full credit. e) Indicate which product is the major and which product is the minor in reactions 2 and 3. Briefly justify your answer.
- I recovered 3 mL of cyclohexene, how many grams of water was produced in the reaction please show how? Cyclohexanol can attack the carbocation intermediate formed during the synthesis of cyclohexene. Draw this side product with the molecular formula C12H22O. Please ASAPPPP you guys didn't answer the last oneObserve the REACTION in the diagram below to answer questions 1. What is the type of hybridization of the carboxyl carbon in the mechanism? a. sp1.5b. sp3c. sp2d. sp 2. What is the IUPAC name of the product? a. Pentanoyl chlorideb. Pentanone chloridec. Pentanoic acid chlorided. Pentanyl chloride 3. The illustrated reaction mechanism is considered __________. a. Concertedb. Continuousc. Step-wised. Unfavorable 4. Which atom in the reaction mechanism is the nucleophile? a. Chloride anionb. Hydroxyl groupc. Methyl groupd. Carboxyl carbon 5. What type of reaction is illustrated in the reaction mechanism? a. Electrophilic substitution reactionb. Nucleophilic acyl substitution reactionc. Electrophilic acyl substitution reactiond. Nucleophilic addition reaction 6. What is the main functional group of the organic molecule? a. Alcohol functional groupb. Carboxyl functional groupc. Carbonyl functional groupd. Aldehyde functional group 7. Aside from the organic molecule, what product is…6. Match the reagents and condition below with the appropriate reactant.You may list a reagent or condition more than once.Reagents/condition (s) : Cl2; CCl4; FeCl3; uv light; NaOH(aq); HCN(g), (i) But-1-ene : ……………………………………………………………..(ii) 1-chloroethane : ………………………………………………………...5(iii)Butane : ………………………………………………………………………(iv)Methylbenzene : ……………………………………………………………..(v) 2-chloro-2-methylpropane : ………………………………………………….(vi)Propanone : ………………………………………………………………….(vii )Ethanal : …………………………………………………………………….