For the substitution (SN2) reaction below circle the nucleophile and draw a box around the electrophile. Then, using curved arrows, draw the reaction mechanism. CH,S acetone Br

Q: CH3CO3H

A: In presence of per acid ,ketone molecule undergo Baeyer villiger rearrangement. Among two alkyl…

Q: Sl2, AICI; a complete curved mechanism -arrow generation of the active electophile 1. Two equivalent…

A: A chemical reaction proceeds in the forward direction by reacting with other molecules of the…

Q: Which do you think is a stronger nucleophile in an SN2 reaction-pyridine or pyrrole? Explain. H.…

A: The complete Lewis structures of the two compounds are

Q: B. CIRCLE (CROSS-OUT) the FASTEST (SLOWEST) Nucleophilic Substitution Br + H3C-O + H3C-O .CI

A: Rate of Nucleophilic substitution depends on the nature of leaving group. Better the leaving group…

Q: Predict the neutral organic product of the reaction. Select Draw Rings More Erase C H H2SO4 но H-O H

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Q: Select one activator & ortho para director to be on a benzene ring to start.  You will then add a…

A: Here, I take -OMe (methoxy) group as an activator.  In case of anisole, the l.p. present on -OMe…

Q: Question attached

A: In the given SN2 reaction, the nucleophile will attack from the backside to the leaving group and an…

Q: How does the strength of the nucleophile affect an SN1 or SN2 mechanism?

A: Given reaction types,     SN1 reaction mechanism     SN2 reaction mechanism

Q: Following Curved Arrows to Draw a Reaction Product Follow the curved arrows and draw the products of…

A: This reaction is an elimination reaction  In which alkyl halide is converted into an alkene with the…

Q: By following the curved red arrows, draw the product(s) of each of the following reaction steps.…

A: a. In accordance with the movement of electrons in the above reaction, bromine atom was detached…

Q: Br Na C: CEN

A: Given reaction,

Q: Construct a three-step synthesis of 3-bromocyclopentene from cyclopentane. Drag the appropriate…

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Q: Draw a detailed mechanism. For each step of the mechanism, jusiuny what you drew/explain the why…

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Q: Rank the following substrates in order from slowest SN1 reaction rate to fastest. Br Br Br Br A В

A: The stability of carbocation is given as substituted with Hetero atom > Tertiary > Secondary…

Q: Circle the least reactive compound from the following in an SN1 reaction: Br Br Br С. В. Br D. O B

A: SN1 reaction is a substitution reaction.

Q: Show how a 1,2-shift forms a more stable carbocation from attached intermediate.

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Q: Which of the following is not a nucleophile? (Circle one answer). a. Н2О b. CH30- ntherate с. NH3 d.…

A: Nucleophile, is  an atom or molecule that in chemical reaction want a positive centre, such as the…

Q: The following reaction is done with a low concentration. What type of substitution mechanism will be…

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Q: Circle the major product in the E1 reaction of the following alkyl halides

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Q: Add curved arrows to each step in the following reaction sequence.

A: curved arrows to each step in the following reaction sequence is shown below:

Q: Drawing the Products of an SN1 Reaction Label the nucleophile and leaving group, and draw the…

A: the nucleophile and leaving group

Q: Add curved arrow(s) to draw step 2 of the mechanism. Modify the given drawing of the product as…

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Q: Why do carbocation rearrangements occur? Choose all that apply. Ring strain can be reduced. They…

A: Carbocation rearrangements are the organic reactions in which the movement of an unstable…

Q: i) (CH3)3N: (CH3)2ö: W ii)

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Q: The nucleophile approaches from the opposite side of the carbon with the leaving group in which…

A: It is SN2 reaction. In SN2 reaction i.e nucleophilic substitution biomolecular,   one bond is broken…

Q: Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and…

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Q: Circle the better nucleophile in polar protic solvent. Below each answer, BRIEFLY explain your…

A: Polar protic solvents are capable of forming hydrogen bonding because they have atleast one hydrogen…

Q: H F LL H LL F F

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Q: Draw all possible products in the following reaction and circle the most stable product. Br КОН ELOH

A: In this question, we will draw all products for this reaction and the circle the most stable…

Q: Drag the appropriate items to their respective bins. CH3 CH= CH2 CH3 CH3CH(CH3)CH,NH2 CH3CH2COO…

A: Attacking reagents can be classified into two types  Electrophiles (E+)  Nucleophiles (Nu-)…

Q: Circle the reactant that is a nucleophile and draw the mechanism using the appropriate arrows for…

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Q: 4. Circle the molecule that would react fastest in an SN2 reaction. In addition, classify cach…

A: The molecules given are,

Q: Show how a 1,2-shift forms a more stable carbocation from each intermediate.

A: The shift occurs in ionic species .and the shift males the carbocation more stable.  In 1st…

Q: Draw the major nucleophilic substitution product of each reaction below, showing stereochemistry…

A: Concept: SN1 reaction :  1. Weak or moderate nucleophile 2. bulky reactant 3. polar protic solvent…

Q: a. Strong bases are [ Select ] nucleophiles. b. Electron-withdrawing groups nearby a nucleophilic…

A: Bases try to abstract hydrogen whereas nucleophiles attack electron deficit carbon atoms. The groups…

Q: From each pair, select the stronger nucleophile. Q.)Cl- or I- in DMSO

A: The species, that make a covalent bond by donates a pair of electrons is known as nucleophile.…

Q: NaNH2 `NH2 CI i) NaNH2 NH2 Br ii)

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Q: For each pair of reactants (A-C) draw all possible E2 products, label each as a mono, di, tri, or…

A: When an alkyl halide reacts with a strong base, the reactants can undergo two mechanisms. The…

Q: CH3 H;C-C-i: CH, CH3 H,C CH,

A: SN1  stands for nucleophillic substitution reaction where rate of the reaction depends on only the…

Q: Br O,N

A: 1. In aromatic electrophilic substitution reaction,  substituent attached with benzene ring controls…

Q: NH2 но. CF3 CF3 IZ

A: The fate of the given reaction is decided by the chemical nature of the leaving group and its…

Q: For the substitution (SN2) reaction below circle the nucleophile and draw a box around the…

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Q: Which reagent(s) will result in the nucleophile attacking the more substituted side of an epoxide?…

A: The question is based on the concept of organic reactions. It involves ring opening  of the epoxide…

Q: In the given condensed formula, I understand that there will be a carbocation rearrangement due to…

A: The E1 mechanism of conversion of secondary alcohol to alkene is given in step two.

Q: From each pair, select the stronger nucleophile. Q.) CH3SH or CH3S-

A: The species which make a covalent bond by donating a pair of electrons is termed as nucleophile.…

Q: Br

A: Under polar and protic solvent in the presence of weak base E1 elimination is favored. E1…

Q: 1. Assuming no other changes, what is the effect of doubling both the alkyl halide and the…

A: SN1 reactions are Nucleophilic substitution reactions. These are unimolecular reactions. Thus the…

Q: Determine whether the sollowing are SN1,SN2, E1, or E2 and draw the major product and if more than…

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Q: Complete the mechanism for the given reaction by adding the missing bonds, charges, nonbonding…

A: An organic reaction can proceed in the presence of acid if the reactant is an ester. In this case…

Q: Draw the curved arrows and the product for each of the following nucleophilic addition steps. (a)…

A: Hi. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If you…