What is the product of the following reaction? Circle the correct answer. NABH, A. B. C. D. Он О Он OH ОН ОН Он

Q: 9. Which SN1 reaction in each pair is faster? a) b) (CH3)3CCI + H2O → H,O (CH3)3CB +H0→ .CI H,O

A: SN1 is a unimolecular Nucleophilic substitution reaction. The reaction involves a carbocation…

Q: Below there are two pairs of compounds. For each pair circle the compound that would react more…

A: E1 reaction is passing through the formation of carbocation intermediate. Greater is the stability…

Q: CH3 Br NaOEt ETOH

A: Bimolecular elimination reaction (E2) occurs in a single transition state and the rate of the…

Q: Draw the product. Select Draw Rings More Erase H HgSO4, H20 H2SO4 -H

A: This reaction is example of hydration of alkyne .

Q: Fill in the missing reagent(s) that would transform the starting material to the final product. (5…

A: Given:

Q: Q3\ Complete the following reactions with appropriate compounds? Ni CH;CH2-C-CH2-CH3 + H2 ?…

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Q: Which product(s) will be formed preferentially in a base elimination? (1) (2) H KOH, EIOH Br Br (3)…

A: Ans

Q: H. 1. NABH4 2. Neutralizing work-up

A: Here a reaction is given .For this reaction reagents and products are given.We have to draw the…

Q: t-BUOK E2 only Br

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. H. 1. NABH4 2. Neutralizing…

A: Addition of hydride as nucleophile to the carbonyl carbon of aldehyde group  Protonation as…

Q: Show the reagents for the conversion below: EtO OEt HO.

A:

Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HO H,SO, Part 1:…

A: This reaction is dehydration reaction which means water leaves out the reactant. Under acidic…

Q: Design a stepwise synthesis to convert cyclopentanone and 4-bromobutanal to hydroxyl aldehyde A.

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Q: MAKE: CEN CEN FROM: or USING ANY REAGENT WITH 42 CARBONS (SHOW STEPS)

A: GIVEN:-

Q: 5. Explain why the nitrogen on the molecule on the left below is more reactive as a nucleophile than…

A: Nucleophilicity depands On negative charge density.

Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: `Br CH3CH2OH Part…

A: Given

Q: Draw a stepwise mechanism for the following reaction: HBr HO, Br Part 1: HOBR Br H,0 HO view…

A: Alcohol reacts with a hydrogen halide to form an alkyl halide. The reaction proceeds with an SN1…

Q: Part 2: Simple Reactions Draw the structure resulting from the following HC1 + HOCH₂CH₂OH CH₂OH Dess…

A: We have to show the major organic products.       N.B. According to the company guidelines, we have…

Q: Provide the synthetic route for the following reaction?  (CH3)2CHCH2Br ----> (CH3)2CHCH2CH2CH2NH2

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Q: OH HO CH3

A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…

Q: Which benzylic halide reacts faster in an SN1 reaction? Explain.

A: From among the two benzylic halide given we can tell that the halide A reacts much faster than…

Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr OH Br Part 1…

A: Alcohol reacts with a hydrogen halide to form an alkyl halide. The reaction proceeds with an SN1…

Q: A concerted, one-step reaction is involved between tert-Butyl bromide and sodium hydride at 50 o C.…

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Q: 2.1 For Figure 4. Determine the products when Figure 4 reacts with the following reagents below.: H…

A: When an aldehyde 4-tert butyl cyclohexanecarboxaldehyde is treated with sodium borohydride then with…

Q: H3C Br H3C CH3 H3C Aqueous ethanol HO CH3 H. H. CH3 BH3 O-BH3 Proton transfer d = El Elimination…

A: The question is based on the concepts of reaction mechanisms of organic chemistry. there can be…

Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr Br Part 1:…

A: The given reaction is an example of the reaction of secondary alcohol with HBr. Generally, alcohol…

Q: XS ㅅ ? HBr Draw the major organic product(s) of the reaction.

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Q: 8. Design a synthesis of the target molecule from the starting material shown. ОН "ОН

A: The given tertiary butyl alcohol reacts with conc. Sulfuric acid and gives 2-methylpropane.  It…

Q: Choose the reagent(s) that would be most likely to complete this reaction. HBr (1 equiv) H2O2

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Q: 1. CH2=CHLI 2. НзО*

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Q: Please help! And show work clearly

A: SN1 reaction is a nucleophilic substitution reaction in which the rate determining step depends on…

Q: Parts A and B A. Circle the molecule with rhe lowest bp. HO, B. Rank from most acidic (1) to least…

A: (A) Boiling point reduces when intermolecular force of attraction weakens. When force decreases,…

Q: Br neo keN SCH,

A:

Q: Provide a synthetic route to the following compound(s) а. Br он from "H b. from SCH3

A: a) Since the configuration of carbon is changing in the product. Hence it means the conversion of…

Q: What are the reagents required to make the following conversions? ? ? a) b)

A: a) SN2 nucleophilic substitution reaction

Q: The SN2 reaction can be best carried out with   A. Primary alkyl halide B. Secondary alkyl halide…

A: The SN2 reaction can be best carried out with --

Q: Part 2 out of 2 Grignard reaction: 1] CH3 CH,MgBr он Select the correct reagent for C. MCPBA NABH4,…

A: In the given question we have Cyclohexanol which is oxidized with PCC(Pyridiniumchlorochromate) to…

Q: The transformation above can be performed with some reagent or combination of the reagents listed…

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Q: LNe Peagent list, identify the reagent needed for each transformation below. The reagent list is in…

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Q: Consider the reaction of an alkyl bromide and hydroxide ion. Br HO- Draw the Sy1 product. Draw the…

A: SN1 reaction is unimolecular nucleophilic substitution reaction. It is a two step reaction and the…

Q: Which halide is most reactive in SNl reactions? Select one: O H;C-CH2-CH2CI CH3 H3C-CH-CH2CI CH3…

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Q: Design a synthesis for the target molecule from the indicated starting material.

A: Given, Reactant = Ethyl benzene  Product = 3-Phenylpropanenitrile  Conversion = ?

Q: Which reaction does not correctly circle the more stable base? A) + CH3 B) + OCH3 OCH3 C) Но + H20 +…

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Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr HO. Br Part…

A: Applying concept of SN1 reaction.

Q: Which solvent is more appropriate for the following SN2 reaction, acetic acid or acetone? SH NaSH ?…

A: Polar protic solvents are capable of hydrogen bonding because they contain at least one hydrogen…

Q: using the starting materials given below. Any reagent needed can be used and you may need more than…

A: Applying concept of organic synthesis and reagent.

Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HO H2SO4 Part 1…

A:

Q: Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr OH Br Part 1:…

A: In the given reaction alcohol is reacting with HBr to give alkyl halide as the product, In the given…

Q: For succeeding items, refer to the image provided. A B CH3C=N 1. Which atom will most like be the…

A: In organic chemistry, there are species that are either electron-rich or electron-deficient.…

Q: What reaction is occurring? Circle one. 1. LIAIH4. -ОН Nucleophilic Substitution Reduction 2. H20…

A: Since LiAlH4 is an strong reducing agent as it produces H- ions in the solution. Hence it reduces…