Q: (i) (ii) NaOH (iii) SOCI₂ heat (iv) CH₂N₂ (2 eq.) (v) Heat, EtNH₂ C12H21 NO2
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Q: 0: Br HO
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Q: What is the major product produced in the following reaction? HO Br CH,SNa CH,OH Но HO но 1) 2) 3)…
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Q: %3D arbocations in order of increasing stability (least stal cures may be equal in energy. II IV V
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Q: -OCH3 -OCH2CH3 Or I II
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Q: DMF water + Nal (a) (b)
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Q: CH3 CH3 OCH, H CHy CH CHs H CH, 3 2.
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Q: Which of these compounds is MOST reactive towards NH₂? Select one: ов D O A OC
A: Since you have asked multiple questions, we will solve the first question for you. If you want any…
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Q: Identify compounds G and H in the following reaction scheme. Hrepresents the structure of…
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Q: Account for the formation of the product and for the cis stereochemistry of its ring junc- tion.…
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Q: 4. The anisole derivative below undergoes a selective cross coupling reaction on only one of the two…
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Q: d) What are the reaction products of the following scheme? Give reasons' Br2 1-ButCl AIC13 :CCI2
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Q: 2. For the following amines A and B, show all of the Hoffman elimination products. If one product is…
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Q: Br NaGN HGN
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Q: Rank the following organobromides in order of increasing rates of ionization to its carbocations and…
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Q: Arrange the following compounds in the increasing order of reactivity in SN' 1. CH3CH=CHCI 2.…
A: In SN1 reaction, the rate of reactivity increases with the increase in the stability of carbocation…
Q: O 1. CH3CH₂MgBr 2. H₂O
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Q: Ethane HCI Br2 Uv H H2O Sulfuric OCH3 B 1 mol h2/ lindlars F Br2 D E 2NaNH2 NaNH2
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Q: Br
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Q: Rank the following organobromides in order of increasing rates of ionization to its carbocations and…
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Q: For the reaction given below, predict which product will be the major one and by what mechanism it…
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Q: 2. For the following amines A and B, show all of the Hoffman elimination produc If one product is…
A: The Hofmann Elimination is an elimination reaction of alkylammonium salts that forms C-C double…
Q: what reagents can you use to connect the cl to the double bond to make it all one product? CI 3D0
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Q: 1. What is the order of increasing reactivity in an SN1 reaction for these compounds? a to Br `Br II…
A: We can look at the mechanism for SN1 reaction to predict the reactivity. At first the leaving group…
Q: Which of the molecules A through D shown below will give mixtures of enantiomers upon reaction with…
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Q: At what pH will Cl3CCO2H dissociate 50% in water? At what pH will it dissociate 90%? At what pH will…
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- Possible alternative brominations include: Veratrole (1,2-dimethoxybenzene) to 1,2-dibromo-4,5-dimethoxybenzene; 4-Methylacetanilide to 2-bromo-4-methylacetanilide; 2-Methylacetanilide (made in experiment S.1) to 4-bromo-2-methylacetanilide; Vanillin to 5-bromovanillin; Acetanilide to 4-bromoacetanilide; a. b. C. d. e. EXPERIMENT S4: BROMINATION OF AROMATIC COMPOUNDS Certain other acetanilides made in experiment S.1 may also be used as precursors in this experiment. Estimated time: 1 afternoon Associated learning goals: Section 6, LG 6.6; Section 7, LG 7.2 and 7.4 Pre-lab report: complete the standard report form, and answer the following questions. In this experiment, molecular bromine (Br2) is generated from the redox reaction of potassium bromate with hydrobromic acid. Write a balanced equation for this process. Briefly outline the mechanism by which Br2 brominates your aromatic compound. Why do the bromine atoms end up at the positions indicated rather than anywhere else in the…Which products are obtained by the following reactions (a) and (b)? Specify the expected main product, if several products can be formed.1. Predict the products of each of the following reactions
- For the reaction shown, seledt the expected major organic product. Pt II IVWhich of the following alkyl halides will react more quickly in the El reaction (d) (b) (c) (a) to to Br Br Br BrCompounds A, B, and C are isomers of xylene (dimethylbenzene). When each of these isomers undergoes a single nitration, compound A produces just one product, B produces a mixture of two products, and C produces a mixture ofthree products. Identify which of compounds A, B, and C is the ortho isomer, which is the meta isomer, and which is the para isomer.