Provide a plausible arrow pushing mechanism for the reaction below. 1. ABuLi ŅME2 2. MgCl HO,C. 3. CO2 4. acidic workup NME2 NME2

Q: Make a table of the physical properties (molar mass, MPT, BPT density and mass used/needed) for the…

A: Benzophenone is reduced to benzhydrol.with NaBH4.

Q: How is this reaction is carry out ? Show all the steps please arrows and all the movement of…

A: The conversion of a primary alcohol to carboxylic acid via aldehyde is the oxidation reaction.

Q: HBr (excess) Br Br

A: Electrophilic addition reaction takes place when alkyne reacts with HBr. Markvnikoff rule for…

Q: Write a detailed mechanism. OH りNaoH 2)Brz in CH2C 2

A: First step of the the reaction is Favorskii rearrangement. This reaction is followed as follows:

Q: 23. Which reaction or statement regarding nucleophilic substitutions is incorrect? A) XCI + 2 H₂O…

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Q: Discuss the mechanism and desirable products of following reactions: ? SH ?

A: Primary alkyl halides undergoes substitution via SN1 mechanism.

Q: 5. Provide the mechanism for the Wittig reaction below. H3C H3C- FPPH3 CH3

A: The  Wittig reaction is the chemical reaction of aldehyde or ketone with a triphenyl phosphonium…

Q: Provide a plausible arrow pushing mechanism for the reaction below. cat. TSOH, A + H20

A: acidic Aldol mechanism  with full arrow steps involved in step-2

Q: Provide a plausible arrow pushing mechanism for the reaction below. O-OtBu s-OtBu AHN. CO,Me 1. LDA…

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Q: Br Mg MgBr MgBr C6H5 MgBr + C6H5 C6H5 C6H5 MgBr H' in H2O C6H5 CgH5 C6H5 C6H5

A: Given,

Q: How does changing the solvent from CH3OH to DMSO affect the rate of an E2 reaction?

A: The reaction in which one molecule is eliminated from reactant compound, such reaction is called…

Q: 3 CH3I NaOH solution NH2 [7] (11) (i) AGOH (replaces I with "OH) (ii) 180 °C [8] (14) (12) (13) 95%…

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Q: Show the mechanism and products formed when the given molecule reacts with NaOD and D2O.

A: When D2O is added in the reaction, the deuterium atom substitutes the proton of hydroxyl group. The…

Q: Br Mg MgBr MgBr C6H5 MgBr + C6H5 C6H5 C6H5 MgBr H' in H2O C6H5 to CgH5 C6H5 C6H5

A: For the above Grignard reagent there is a possibility tto form biphenyl as a byproduct or side…

Q: CF2Cl2 can be prepared from the nucleophilic substitution of another alkyl halide CCl4 in the…

A: Given-> CCl4 + 2HF ------> CF2Cl2 + 2HCl.  Rate = K[CCl4] Rate constant (K) = 1.5 × 10-4 s-1…

Q: Why is tertiary carbocation most favored for Sn1 reactions?

A: In this question, we will discuss about why SN1 Reaction is more favored for Tertiary carbocation.…

Q: What is the predominant mechanism of the reaction below? Br NaOCH3 CH3OH SN2 El E2

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Q: 'Bu CN Ph Br NB: 'Bu =

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Q: Worksheet 9 – Chapter 8 Given the information below, write out a reasonable mechanism for the…

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Q: The E1 mechanism (unimolecular elimination) of Elimination ?

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Q: Consider the following reaction: КОН + KBr Br OH a) Does the reaction proceed via an SN1 or SN2…

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Q: M5 Explain the different stages of reaction, reaction mechanisms, conditions of reactions, (for the…

A: M5)A reaction takes place in different stages for example lets take a second order reaction it…

Q: DMF water + Nal (a) (b)

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Q: The diagrams 1 to 3 below can be arranged to show the mechanism involved in a familiar reaction. The…

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Q: For each of the following reactions, predict the major product. 1. SOCI2 2. H2N (еxcess) HO, mCPBA…

A: 1) Reaction of carboxylic acid with SOCl2 produces acid chloride. Reaction of acid chloride with…

Q: b) Complete the following reactions. i. `NH2 „NH2 SOCI, i. iii. LIAIH4

A: In organic reaction, the reactants are organic compounds, the reaction mechanism depends upon the…

Q: он Br

A: Given reaction,

Q: β-elimination reactions.

A: IN E2 REACTION THE H WHICH IS SITUATED IN BETA POSITION ARE ABSTRACT BY BASE AND ALKENE IS FORMED…

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1.1 eq. 1BUOK HO 2. acidic…

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Q: Which step in the following reaction will cause the proposed synthesis to fail? A B .CI NBS -Br…

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Q: In each reaction box, place the best reagent and conditions from the list below. 1) 2) 3) 4) PB 3…

A: The given reaction can take place as follows:

Q: Using your class average data, compare the following alkyl halides for the SN1 and SN2 reactions: Br…

A: The rate of an SN1 reaction depends on the stability of the intermediate carbonation and the rate of…

Q: Provide a plausible arrow pushing mechanism for the reaction below. 1.1 eq. tBuOK 2. acidic workup

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Q: 2. Consider the following reaction called hydrovinylation from homework # 4: Clearly sketch out the…

A: Mechanism shown in step 2.

Q: 01. Of the following statements, which are true for nucleophilic substitutions occurring by the SN1…

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Q: 1) Compare and contrast the Type 1 electrophilic addition to the unimolecular substitution and…

A: The SN1 reaction involves two separate steps: first the departure of the leaving group and then the…

Q: It will be helpful if I find the distinction between these two products since they are both…

A: The given molecule:

Q: CO,Et co-Et i. NaH ii. Br ii. NaOH/H,O, heat iv. H;O“, heat v. SOCI2 vi. AIC13

A: Nucleophillic Substitution reaction (SN2): These are the reactions where a stronger nucleophile…

Q: Define mechanism for LiAlH4 Reduction of RCHO and R2C=O

A: Lithium aluminum hydride, LiAlH4, also abbreviated as LAH, is a reducing agent commonly employed in…

Q: 3. Explain why the treatment of ferrocene in this reaction yields two products and offer an…

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Q: what is the Nature of the leaving group (LG)?

A: Leaving group :-        It is group or atom or molecule which is completely displaced by other…

Q: 4. For the Sn2 reaction below: Give the mechanism with curved arrows and products for the reaction…

A: Given:

Q: 1. Complete the reaction and indicate how IR spectroscopy could be used to monitor the reaction…

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Q: Draw the structures of the starting material and the four missing intermediates. OH allyl bromide,…

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Q: Do all primary iodides react with N 3 - at the same rate via the S N2 mechanism? Explain.

A: Rate of the SN2 reaction is depends upon many factors such as:-

Q: Provide a plausible arrow pushing mechänism fof the ОН OMe TSOH, H20 OMe

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Q: 1. what is the Nature of the leaving group (LG)? 2. what is the relative size of activation energy…

A: A leaving group always removed from the species  with the bonded electrons.

Q: When hydroxide is used as the base to carry out an E2 reaction on a vinylic halide, the reaction…

A: E-isomer:  In an alkene if both the group along double bond is in opposite side is called E-isomer.…

Q: Provide the mechanism for the 2nd reaction in this synthesis: D2S04 PSO4

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Q: For each reaction, give the expected solution product and predict whether the machanism will be…

A: a) 2-chloro-2-methylbutane + CH3COOH The reaction of 2-chloro-2-methylbutane with acetic acid takes…