Explain why the following are NOT the products you would predict for a one-step nucleophilic substitution reaction, and draw the correct product/s. (Note: Na* is a spectator ion.) H3C H3C Na Na HO: CH2CH3 CH2CH3
Q: Draw a reasonable mechanism for the following reaction HO-S=0 HO OH OH
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Q: (Rank each of the molecules from least to most nucleophilic with 1 being the least four being the…
A: In chemistry, a nucleophile is a chemical species that forms bonds with electrophiles by donating an…
Q: OH H2SO4 HOCH,CH3 Doubling [CH3CH,OH] doubles the rate of rxn.
A: Given : Doubling concentration of CH3CH2OH doubles the rate of reaction.
Q: the reaction below, which face of the carbonyl did the nucleophile (SH) add to? HS O SH
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Q: Identify the stronger nucleophile in the following pair ? CH3NH2, CH3OH
A: The CH3NH2 has a lone of electron over the amine which is unhindered and won’t not donate the…
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Q: LOH (RL NaOH (S) H2O This nucleophilic substitution occurs with rearrangement. Draw curved arrows to…
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Q: Consider the intramolecular nucleophilic substitution reaction shown here. Does the stereochemistry…
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Q: Identify the stronger nucleophile in the following pair ? CH3CO2−, CH3CH2O−
A: A nucleophile has a negative charge on it which means it consist of a lone pair of electron for…
Q: Question is attached
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Q: Rank the nucleophiles in following group in order of increasing nucleophilicity. H2O, −OH, CH3CO2-
A: Water is a weak nucleophile because it is neutral. Since acetic acid is more acidic than water, the…
Q: OH H2SO4 (cat.) H20
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Q: Complete the mechanism for the following reaction by adding the missing bonds, charges, nonbonding…
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Q: Which of the following correctly represents a nucleophilic attack? :o: :CN ö: : :CN ..O :
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Q: H NH2 H* H OH H H Step 1. H H* Step 2.
A: Amine is nucleophile and it can attack at electrophilic center.
Q: Which product shown is the correct product formed in this multi-step reaction? Acetic Acid Chloride…
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Q: When a single compound contains both a nucleophile and a leavinggroup, an intramolecular reaction…
A: When nucleophile substitutes a leaving group, such reactions are called nucleophilic substitution…
Q: Q10. For each of the following reactions (a-b), predict whether the substitution is more likely to…
A: SN1 is Unimolecular substitution reaction occurs in presence of weak nucleophile and tertiary alkyl…
Q: Draw the products that result from the following bimolecular nucleophilic substitution (SN2) step.…
A: In SN2 reaction ,there is no intermediate form and inverted product is obtained.
Q: 0° CN is a nucleophile . hence it strong undergo SN2 Kh. CN CNO SN2
A: Both the anions undergo substitution reaction because both are good nucleophiles and good…
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Q: Rate the below nucleophiles in terms of INCREASING nucleophilicity. Explain why. CH3OH CH;0 t-BuO-…
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Q: Q10. For each of the following reactions (a-b), predict whether the substitution is more likely to…
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Q: For the substitution reactions below, draw out the reactions as shown and answer the following…
A: Applying concept of organic synthesis.
Q: Provide a complete mechanism for the following reaction. Use curved arrows to depict electron each…
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Q: This molecule will undergo a bimolecular nucleophilic substitution reaction with hydroxide ion. Draw…
A: In SN2 (bimolecular substitution reaction), alwase inverted product is formed.
Q: A nucleophilic substitution reaction is shown below. Identify the nucleophile. I A) CH:S- B) Na II…
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A: Given, Draw the mechanism = ?
Q: 5. The reaction below proceeds through a 4-step mechanism. Classify each step according to the…
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Q: Draw the configuration(s) of the substitution product(s) formed from the reaction of the following…
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Q: "ropose a mechanism for the following reaction. но H,SO, + H,0
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Q: - + ELOK ác. acético DMF CH CH:ONa CHOH CH3 t-BUOK, A CH3 HạC Br CH3 MeOH CH3
A: Recall the conditions of nucleophilic substitution reaction wheather unimolecular or bimolecular.
Q: ö: Br: H,0 heat ОН DH
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Q: Identify the nucleophile in the reaction below: *
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Q: Draw a plausible mechanism for the reaction. CH-OoC,,H35 CH-OH 3 NaOH 3 CH-OO C17H35 CH-OH Nao…
A: ->-OH is nucleophile hence, give nucleophilic addition elimination reaction.
Q: CH2- HI
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Q: Please explain the mechanism of the following reaction and why these products are formed in the…
A: Organic reaction mechanisms:
Q: НО H2SO4 heat
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Q: For each of the following reactions, determine which ELIMINATION mechanism (E1 or E2) will occur.…
A: Elimination reaction: E1 elimination reaction with major product
Q: .CI AICI, 'CI 'CI
A: Ans Electrophilic substitution reaction takes place
Q: a) Dissociation of sodium chloride b) Addition of hydroxide ion to acetone c) Formation of potassium…
A: The electron pushing arrows, bonds and lone pairs are shown in the following step.
Q: CH3-Br Ag,0 C5H13N N(CH3)3 H20 (heat) (еxcess)
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Q: CH3 t-BUOK, A CH3 HạC Br Cl CH3 MeOH CH3
A: - t-BuOK is strong base more than a strong nucleophile hence favors the formation of eliminated…
Q: When a single compound contains both a nucleophile and a leaving group, an intramolecular reaction…
A: Intramolecular reaction is that reaction which takes place within a single molecule.
Q: Draw the product and the complete nucleophilic substitution mechanism (all curved arrows) for the…
A: the reaction mechanism is provided below in attach image.
Q: Rank these substrates in order of increasing ability to undergo a nucleophilic substitution aromatic…
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- Answer the question below the reaction. ta The reaction above proceeds through which type of mechanism? SN2 SN1 E1 E2 OH + Excess NH4C1 H₂SO4 + H₂ODraw a detailed, step-wise mechanism for the reaction shown below. SHOW ALL BOND-FORMING AND BOND-BREAKING STEPS. SHOW ALL INTERMEDIATES. 1) NaOH 2) H3O* H3C H3C HOH3C-C O: H ethanal :CN: and the electrophile is cyanide ion In the step you have just written, the nucleophile is slow rate-determining Ö—0—1 H3C-C-C=N; adduct
- Draw the favored product(s) of the following reactions (organic chemistry)In an E2 mediated elimination reaction of an alkyl halide (H-X) using NaOCH3 as base, which of the following statement is not true? O The reactivity order for alkyl halides (RX) is tertiary secondary> primary. O The rate of reaction = k2 (alkyl halide] [NaOCH₂] O The reaction occurs in a single step. O The rate is independent of the leaving group.Draw the products of the two step reaction sequence shown below. Ignore inorganic byproducts. If the reaction results in a mixture of ortho and para isomers, draw only the para-product. HNO3 (1 equiv) cat. H2SO4 ✔ Please select a drawing or reagent from the question area
- The products in the following reaction are incorrect, briefly explain why the products are incorrect. oo OH + CH3CH3NHCH₂CH3 H₂C CH₂ CH3 + H₂ORank the set of compounds in order of reactivity (fastest to slowest) in a nucleophilic addition-elimination reaction with a nucleophile such as CH3NH2.The compound below can be prepared with an alkyl iodide and a suitable nucleophile. Identify the alkyl iodide and the nucleophile that you would use. For an anionic nucleophile, you do not need to draw the counterion. Alkyl iodide: OH Draw Your Solution Nucleophile: Draw Your Solution SUPPORT
- Draw all products, including stereoisomers, in the following reaction. CH3 CH,COO Part 1: Identify which mechanism(s) the reaction will undergo. Syl D Sy2 SN2 El O E2 Part 2: The number of S1 product(s): 1 The number of El product(s): 2 Part 3 out of 3 The Syl product: draw structure ... CH: The major El product: edit structure #33 The minor El product: edit structureFill in the missing structure(s) for the reaction pathways shown below. Provide allstarting material(s), reagent(s), or product(s). If more than one product can be formed,draw all major products. If more than one starting material or reagent is possible, writeall starting materials and reagents.Use the reaction given below to answer the following questions. A CH₂OH B H₂O+ C + CH3NH3* D a) What are the approximate pKas of compounds A and B? b) The reaction given above is irreversible. Give a detailed explanation of the reaction and reaction mechanism. Your explanation should indicate your knowledge of the reactivity of carboxylic acid derivatives.