Predict the electrocyclic products of the following transformations, indicate the type of reaction and justify the stereochemistry. CH3 CH3 b) hu A Br hv CH3 A NC =-CN hu
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Q: "OCH; acetone H3C
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A: As per guidelines only 1 question can be answered.
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A: In this quesS-1,3-dimethylcyclohexenetion, reagent and starting material are given, and we want to…
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Q: NaSH acetone 12. НзС H3C H3C° CH3 (n) CI NaSH in H,O 13. (0)
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A: The answer js given as follows
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Q: Predict the major products of the following reactions, including stereochemistry.(a) cyclohexene +…
A: (a) Given: cyclohexene + KMnO4>H2O (cold, dilute)
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Q: `CH3 + HCI → ? CH3CH2CECCH2CH3 + H2O/H2SO4 → stable structure 3-hexyne + 1 mole of Br2 → ?
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Q: NH: (еxces) OCH, (CH;CH;CH,)CuLi
A: Given: Reactions To find: Complete the given Reactions Solution: when ester react with primary…
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Q: Following are two diastereomers of 3-bromo-3,4-dimethylhexane. On treatment with sodium ethoxide in…
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Q: Predict the major products of the following reactions. Include stereochemistry whereapplicable.(a)…
A: Given information: 1-methylcycloheptene + BH3/THF, then H2O2, OH-
Q: CH3 CH3ONA 8. H D. H20 Br 9.
A: The product that form in 8 is shown below.
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Q: H2O 4.
A: Organic stereochemistry of SN1 reaction. Major product is inversion in configuration.
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Q: КОН Br ОН 2.
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Q: 5. Predict the products of the following reactions and propose a mechanism that explains the…
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Q: 1. Predict and draw the structures of the product(s) of the following reactions. If more than one…
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Q: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when…
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Q: Predict the products of the following reactions. Draw the products. Show the stereochemistry when…
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A: Reactions of 1-Methylcyclohexene
Q: (а) H,O, H,SO, (b) Br, H,0 (c) (1) ВН, THF (2) NaOH, H,O, (d) Br. e) (1) O, (2) Мо,S
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Q: Predict the products for each of the following reactions and provide an explanation for the…
A: Diels alder reaction is [4+2] cycloaddition reaction . In which one reactant is diene and other is…
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Q: CH3 + HCI → (a) (CH3),CHCH,CH,CH,CH=CH2 1. 2. + HBr (with peroxides) → (b)
A: Solution of question 1 and 2:
Q: Predict the products of each reaction below. Indicate regiochemistry and stereochemistry when…
A: We have to write the major product of the reaction
Q: а) b) 1. Оз 2. Zn, H20, H+ 1. ВН3, ТHF 2 но, Naон 2 2 CH2 c) H3O*
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Q: H. Br EtO H. THF 10. Me Ph CI 11. EGN+ CH;CH;0 12. ČI DMF
A: Given reactions,
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A: Three questions based on halogenation of alkenes, which are to be accomplished.
Q: 1. Me 2. NaH, DMF `CI, py, CH2Cl2 Br OEt NH2 3. H20, H*, heat 4. CP2LANME2, PhH
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Q: Predict the Product of the reaction and indicate regiochemistry and stereochemistry when relevant.…
A: Ozonolysis:Alkene reacts with ozone which cleaves the double bond followed by work up with zinc and…
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Q: Predict the major products of the following reactions. Include stereochemistry whereapplicable.(a)…
A: (a) 1-methyl cycloheptene + BH3, THF, then H2O2, OH-(b) trans-4,4-dimethylpent-2-ene + BH3, THF,…
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- Predict the final product(s) obtained when (2R,3R)-2-bromo-3-methylpentane is subjected to the following sequence of reactions, briefly explaining your rationale. For each step, provide the stepwise mechanism and the regiochemical and stereochemical details as relevant. 1. NaOC2H5/C2H5OH, heat 2. BH3, THF 3. H2O2, OHwrite the mechanism and predict the product, and includ the stereochemistryWrite the mechanisms of the following reactions and examine the products as stereoisomeric.
- Suggest a detailed mechanism for the reaction below. Represent the product in the most stable conformation and also its stereochemistry (Identify stereogenic centers as R or S)Predict the products of the following reduction reactions, including stereochemistry where needed. If the reaction product is racemic, indicate that by writing “racemic”. please explain stepsCyclohexene reacts with bromine in the presence of NaI to yield -?
- Write the mechanisms of the following reactions, describe the products as stereoisomeric. A ,B , C , D , E , F=?Please find the major products include stereochemistry if relevant. State if there are enantiomers. Thanks!Can you assist with predicting the organic product(s) of each of the following reactions and provide stereochemistry, if applicable.
- What is the most likely product, I, II, III, IV, of the following reaction with correct stereochemistry?Predict the major products of the following reactions, and give the structures of any intermediates. Include stereochemistry where appropriate.The given are attached below:Bromine reacts with alkenes in methanol according to the equation: - When this reaction was carried out with 4-tert-butylcyclohexene, only one isomer was formed with the molecular formula C12H23BrO (80% yield). Which of the following is the structure more reasonable for this compound?. Explain your reasoning through acorresponding mechanism.