Which of the reactions below are correctly identified?     These are SN2 reactions:

Q: Draw the products of the following reactions, including their configurations:

A: Asymmetric center or chiral center is the sp3 hybridized carbon center that is connected to four…

Q: OH a) (R)-2-Bromobutane 25°C b) 3-Bromo-3-methylhexane MEOH 25°C I c) t-Bu Asetone, 50°C

A: First three can be answered. Please resubmit the question with other parts.   Several factors…

Q: Which pathway will this reaction likely take? NaSH ? SN1 O SN2 O E1 E2

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Q: c) t-Bu Asetone, 50°C N3 DMF Br NaCN e) Br DMF

A: I and Br and Cl are good leaving groups and N3- and I- and CN- are good nucleophiles as well as a…

Q: Which of the compounds below is the major product of the following reaction Cr203 но HO. HH;0 OH OH…

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Q: Which of the following is considered to be a thermodynamic product of the reaction shown. DBr OA OB…

A: Diene shows the electrophilic addition reaction such addition of X2, HX etc. The addition of HX to…

Q: H CH3ONA ? CH3 Br CH;OH H H H OCH3 CH30 ČH3 OCH3 ČH3 H Br I II III An equimolar mixture of I and |…

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Q: Give the mechanism of the following reactions. Briefly explain why any selectivities occur. 1 eq HBr

A: Ring opening reaction.

Q: Aldol Condensation Product Ph Aldol Addition Product

A: In the question we have been provided with two reactions, one is aldol condensation and other is…

Q: CH,CH,CHCH,, CH,CH,CH,CH,Br, (CH,),CCH,CH, and CH,CH,CH,CI Br CI

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Q: Provide the product and mechanism for the reaction: ОН CrO3, H,SO, H,0

A: This reaction is an example of Jone oxidation. Mechanism of Reaction:

Q: Rank the following in order of increasing reactivity in an SN1 reaction. Br Br Br 1 2 3

A: Given three bicyclic organic bromides. Determine their reactivity towards SN1 reaction.

Q: HCI (conc) it

A: The electrophilic addition reaction of alkene proceeds in two steps. In the first step the proton…

Q: Predict the major product of the reaction K½Cr,O7 HO, H2SO4

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Q: What product or products are produced in each of the following reactions? By what mechanism ( SN1,…

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Q: Write the products of the following SN2 reaction: SN2 OCN + CH3B" Write the mechanism.

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Q: Account for the difference in the products of the following reactions:

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Q: a-1(R)-2-Bromobutane OH 25°C -)(5)-3-Bromo- 3- methyl hexane MeOH 25°C CI -Bu Asetone, 50°C

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Q: OCH3 OCH 3 H₂O* 2 HOCH₂

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Q: Propose a plausible mechanism for the following transformation: [H3O+] HO H EtOH 19.55 The first…

A: Given is a reaction of conversion of 5-hydroxypentanal to 2-ethoxytetrahydro-2H-pyran.

Q: он (1) Hg(OAc)2, H2O OH но. (2) NaBH4lethanol OH (A) (B) (C) (D) Compounds A, C and D Compound B…

A: In this question, we want to determine the Products for this reaction.  How we can determine, you…

Q: КОН Br +

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Q: Compound X, shown below, spontaneously reacts via an intramolecular SN2 to produce intermediate Y,…

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Q: 8.90 ● Suggest an efficient synthesis for the following transformation: OH a- &.. +En Br I

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: What is the synthesis and mechanism for the following?

A: Hofmann's Rule: It is elimination reaction in which the formation of alkene from rather most…

Q: (i) heat molecule N (ii) CO2ET hn heat molecule o molecule P (iii) H- heat molecule Q H- (iv) Ph.…

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Q: The three compounds shown below have increasing reactivity to SN1 conditions from left to right.…

A: In SN1 reaction , there is formation of carbocation intermediate. And rate of reaction depends upon…

Q: Predict the product for the following SN2 reaction. Na

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Q: Please arrange the following according to increasing reactivity towards SN2.

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Q: H* HO, HO

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Q: Acid-catalyzed a-halogenation is a useful reaction for synthesis, especially regarding substitution…

A: Br2 , H3O+ converts Aldehyde to alpha substituted bromide by doing enolisation .