Q: Ph. OTs OTs NaOH NANH, ? ? NaOH ? A В C Ph. CI NaOH dilute NaOH ? D
A:
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Q: Rank the following nucleophiles in order from slowest SN2 reaction rate to fastest if DMSO is the…
A: Given nucleophiles are;
Q: (a) Propose a mechanism for reaction A, which is a substitution reaction. (b) Explain why reaction B…
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Q: 2. Draw the mechanism for this reaction H2SO4
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Q: Rank the following substrates in order of increasing rate of the E1 reaction. NH2 F OTs D A B
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Q: NaN3 Br
A:
Q: 8. Rank the following attacking species in order of slowest reacting to fastest reacting in an E2…
A: E2 represents bimolecular elimination reaction. It completes in a single concerted step. The rate of…
Q: (b) Propose a complete mechanism for the following reactions. (i) Brz, FeBr3 Br (ii) H*
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Q: 1. For each of the following pairs of SN2 reactions, indicate which reaction occurs faster: a)…
A: “Since you have asked multiple question, we will solve the first question for you. If you want any…
Q: Draw the reaction product for the following E2 reaction: Br DBU
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Q: What mechanism did the reaction undergo? KOH ethanol Select one: a. SN1 b. E1 C. SN2 d. E2
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Q: Sy1 A -Br + Br Syl -Br Br -Br Br +
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Q: By what mechanism is the major product of this reaction formed? KCN what mechanism ? a) SN2 b) SN1…
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Q: 5. Draw a detailed arrow pushing mechanism for the following reaction. Is the rate-determining step…
A: When No carbocation is formed then reaction is SN2.if carbocation is formed then reaction is SN1
Q: (a) Draw the structure of molecule (A) that is in equilibrium with molecule (B). (b) Show a…
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Q: What mechanism is involved in the reaction below? CH3 CH3 H₂C- H₂C SN1 E2 E1 C. d. SN2 a. b. CI +KCN…
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Q: 1 .CO2CH CO2CH3 H20 | H2SO4
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Q: 1. For each of the following pairs of SN2 reactions, indicate which reaction occurs faster: CH;CH;Br…
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Q: 0° CN is a nucleophile . hence it strong undergo SN2 Kh. CN CNO SN2
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Q: 16) Which of the following is an E2 step? : NH, :OC(CH,), :0: MgBr Br: II IV a. d. IV b. П e. V
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Q: rate determining step for each an E1 and an E2 reaction including intermidiates /
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Q: Which of the following would be the worst solvent for an SN2 reaction (slowest rate)? N. 0=
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Q: c) Propose a mechanism for this reaction. BF3 Но HO.
A: BF3 , boron triflouride is lewis acid. So lone pair of oxygen of -OH group attack on it and…
Q: 46. What mechanism is/are involved in the reaction below? ho oto hich Осн, NaOCH, a. SN1 & EI b. SN1…
A: Introduction : As per company norms we cannot answer more than one question .So, I am answering…
Q: 24. Which of the following bases would make an E2 reaction occur at the fastest rate? ONa KCI KBr SK…
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Q: Draw the major nucleophilic substitution product of each reaction below, showing stereochemistry…
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Q: Which SN2 reaction will occur most rapidly? (Assume the concentrations and temperaturos are all the…
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Q: Could the reactions shown here take place by a concerted mechanism?
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Q: An SN1 reaction is shown in the box; the reaction profile for this reaction is shown below. Identify…
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Q: ? Br What is the best reagent for the transformation shown above? B E „Mgl A D PPH3
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Q: Draw a plausible mechanism for the reaction shown below. Et Me OH "Me 1) Excess EtMgBr 2) H20 'CI Et
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Q: When Is the Reaction SN1, SN2, E1, or E2?
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Q: OTS NaOH ? A Ph. J dilute NaOH D OTS ? B NaNH, ? E NaOH ? NaOH
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A: We have to identify the what mechanism for the given reaction shown as step 2
Q: Which elimination reaction in each pair is faster? 义ー人 OH OH А. DMSO CI H20 CI H2O
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Q: Which mechanism gave the main product in the reaction shown in Figure 8? * A- SN1 B- SN2…
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Q: Br H,0
A: Br^- is a good leaving group. But, H2O is not at all a base. Rather it is a weak but a nucleophile.…
Q: Propose a mechanism for the reaction shown below. ÇI OH ONH2 + CI Нeat NO2 NO2
A: NOTE: The product given is incorrect and the correct product will have NH2 group in the place of OH.…
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- Rank the nucleophiles in each group in order of increasing nucleophilicity. a.−OH, −NH2, H2O b.−OH, Br−, F− (polar aprotic solvent) c.H2O, −OH, CH3CO2−Which nucleophile in each pair which would give the faster SN2 rate? (a) (CH3)2S or (CH3)2Se (b) (CH3)3CO- or CH3O-Rank the nucleophiles in each group in order of increasing nucleophilicity.a. -OH, -NH2, H2Ob. -OH, Br-, F- (polar aprotic solvent)c. H2O, -OH, CH3CO2-
- Rank the following E2 reactions in order of increasing rate. Show the final product.Which compound reacts fastest in an E1 rxn. The correct answer is C but explain why it is correct and why the other options are incorrect. thanks :)Select which molecule is the better nucleophile in the following pair: a). Br− or Cl− in H2O b). CH3O− or CH3OH in H2O c). HO− or HS− in H2O d). I− or Br− in H2O