QUESTION 18 Consider the ether cleavage reaction shown below. What mechanism occurs and what are the major organic products of the reaction? 1 eq. HCI O A. Mechanism: SN2, Products: OH B.. Mechanism: SN1, Products: OH OC. yo Mechanism: SN1, Products: 'CI HO D. Mechanism: SN2, Products: CI Hot

Q: Draw the products of each reaction. CH2CHCI2 NANH2 NANH2 c. CH3-C-CH,CH3 а. (2 equiv) (excess) CH3…

A: (a)   (b)   (c)   (d)

Q: camparing vanious alkyl halides reactivity toward SN1 reactions using water as a nucleopnile Entry #…

A: Here we have to explain the better leaving group from the given experimental data of SN1 reaction in…

Q: Synthesize the following compound from cyclohexanol, ethanol, and any other needed reagents. HO Part…

A:

Q: Draw a stepwise mechanism for the following reaction: HO H,SO,

A: protonation of alcoholic group loss of leaving group carbocation rearrangement  deprotonation…

Q: raw a stepwise mechanism for the following reaction: Br CH3CH2OH

A: This given reaction is based on williamson ether synthesis. This reaction proceeds via SN2 path.…

Q: Devise a synthesis of each compound from an alkyl halide using any other organic or inorganic…

A: Synthesis of given compunds from alkyl halide are as

Q: Which undergoes electrophilic substitution on the ring most rapidly? a. b. OH CHO d. е. O b a

A:

Q: 1. Give the mechanism and the major product for the reactions below. a. CI NaOH !!!!OH EZONLY

A: Given is E2 reaction. E2 reaction is bimolecular elimination reaction. It is anti elimination…

Q: Synthesize each compound from toluene (CgH,CH3) and any other organic or inorganic reagents. a.…

A: Hey, since you are posted a question with multiple sub-parts, we will answer first three sub-parts.…

Q: stereoisomers. NaOEt 1. Br NaOH Br 2. NaOtBu 3. A Меон 4. Br 2. Which reaction will proceed faster A…

A: 1) Elimination 2) SN2 reaction 3) Elimination  4) SN1 reavtion Reavtion B is faster than A due 1,3…

Q: What is the final organic product in the following sequence of reactions? da Oll O III ON HO. OV H*…

A: The given reaction sequence consists reactions of carbonyl group. At first ketone group is protected…

Q: Devise a synthesis of each compound from cyclopentane and any other required organic or inorganic…

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Which best describes the major isolated organic product of the reaction shown? A) B) 1. BH3 2, H₂O₂,…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: 8) Identify the nucleophile and electrophile in each reaction. А. H. O.. CI CI B.

A: Electrophile : As the name specify electro means electron and phile means loving, it means the…

Q: Q2. Classify the following reactions to: 1. Wagner- Meerwein rearrangement 2. Pinacolic…

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Q: The reaction will proceed with mechanism because the secondary alkyl halide react with nucleophile.…

A: The given 2-bromobutane is a secondary alkylhalide as bromine is attached to secondary carbon atom.…

Q: Draw the major organic product for each of the hydroboration-oxidation reactions. Disregard…

A: Hydroboration–oxidation reaction: Alkene gives an electrophilic addition reaction with borane.…

Q: can you please draw the mechanism to form the product shown? OH Ме, OH B. 1. CrO3, pyridine, H2O 2.…

A:

Q: 3. a. Draw the structures of both of the major products for the following reaction. + H-CI b. Draw…

A: Alkenes undergo addition reactions to form alkanes or substituted alkanes. The reaction of an alkene…

Q: - Mechanism cat. TSOH H. CH3OH

A: Applying concept of  cross aldol reaction in presence of acid.

Q: 3. Show the reasonable curved mechanism for the reaction and make sure lone pairs Y Ocuk + Conc HBr…

A: (a) Lone pair of oxygen is acting as a HOMO and antibonding orbital of H-Br bond is acting as a…

Q: 1. HC=C: Li HC=CH LICI 2. HO HO-S -CH3 Aqueous -CH3 acetone d = Electrophilic a = Proton transfer g…

A: Applying concept of organic synthesis.

Q: Determine the mechanism of nucleophilic substitut a. Br + -CN acetone b. + -OCH3 C. + CH3OH Br H Br…

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Q: A Ph₂N a B O a. 1. NaH; 2. BH3, H₂O O b. 1. NaBH4; 2. HCI, H₂O O c. 1. NaOH; 2. NaBH4 O d. 1. BH3;…

A: The conversion of ketone to alcohol is an example of a reduction reaction. Here, two H atoms are…

Q: 4a. Which of the following is the major product of the following elimination? OMe CI CI A. Ans: Ans:…

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Q: TIOH (cat.) aq acetone Me

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Q: 4. det erMIne ene producu show Stepwise mechanism ant

A: In this question we have to tell the product of the reaction and mechanism.

Q: Draw a stepwise mechanism for the following reaction: H,SO, Part 1:

A:

Q: For the following compound: HO Draw a mechanism for the tautomerization process under BASIC…

A: Given,

Q: For the following compound: HO a Draw a mechanism for the tautomerization process under BASIC…

A: Keto enol tautomerism is a type of structural isomerism. A chemical equilibrium between the keto and…

Q: Which compound is the major product of the reaction below? QH (1) LIAIH, /ether (2) H* (dil.VH,O (A)…

A: LiAlH4 is an reducing agent, it will reduce ketones to alcohols . In reduction H is added while O…

Q: Which alkene cannot be converted into an alkyl bromide with HBr, ROOR, hv, A? 1 11 IV A. B. C. D. E.…

A: 1. HBr addition to alkene in the presence of peroxide will Anti Markonikov product. 2. i. Allylic…

Q: What is the major product of the following reactions? N2OCH3 H20+ ? a. O b. none of the other…

A: Claisen condensation: The Claisen condensation is an example of a carbon-carbon bond-forming…

Q: Consider the following nucleophilc substitution. LOCH3 Br OCH3 в A a. Identify the reaction…

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Q: 1. Steric hindrance is the unfavorable electron-electron repulsion that results when bonds are…

A: Given  bromoethane  2-bromopropane To be determined = sN2 Mecahnism and rate

Q: write mechanism ? CN O H 1. HO. 9 OH H+ (1 equiv.) 2. a) LIAIH4 3. H+ b) H₂O work-up

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Q: Which reaction intermediate (A or B) is more likely to form in the epoxide ring opening reaction?…

A: Epoxide Ring will be open in such way that stable carbocation will formed

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Sn/HCI NO₂

A: -> Sn/HCl is reducing agent which can reduce Nitro group to amine .