Ethylene oxide is the starting material for the synthesis of Cellosolve, an important industrial solvent. Propose a mechanism for this reaction. Н,С— -CH, + CH,CH,ОН H,SO,, CH,CH,OCH,CH,OH 2-Ethoxyethanol (Cellosolve) Oxirane (Ethylene oxide)

Q: Which one is sn1 or sn2 and state the mechanism?

A: -> In presence of polar aprotic solvent there occur SN2 mechanism. -> In presence of polar…

Q: The following reactions give two different products. Shows the mechanism leading to their formation.…

A: For the ring opening of epoxide there is a rule ,  1) When the reaction is performed in the…

Q: H2N- -ОН HO SOCI, Ме ОН Ме Ме

A: Given,

Q: +ОН 1 сн он (Cat) + OH-OH Provide the step by step mechanism (with arrows) that explains this…

A: What you're solving for The step-by-step mechanism that explains the transformation ⁠LEGEND: cap =…

Q: СНЗ — СН— О - СН- СH2 — СНЗ CH3 CH3

A: In a chemical reaction; the substance which involves in conversion is said to be reactant whereas…

Q: NaBH4 МеОн NaBH4 MeOH Pt 3 atm H2

A: Here I have drawn the products for the following reduction reactions.

Q: Which set of starting materials could be used to prepare the following compound in one step? * Meo-…

A: Given product is a diels-alder product . In diels -alder reaction conjugated diene reacts with a…

Q: Propose a mechanism for this reaction and account for its regioselectivity. CH CH3 CH3-C=CH, + ICI…

A:

Q: لمد HO HO.

A:

Q: Synthesize the following compounds from the indicated starting material. OH a) Br Ph OH b) Br CHCH3…

A: Given first two product we can get by grignard addition reaction. And last can be get by elimination…

Q: CI CN NaCN H3C CH3 H3C CH3

A:

Q: CH-CH, CHCI, Show the mechanism step by step to obtain the product

A: We are authorized to answer one question at a time, since you have not mentioned which question you…

Q: Give a reasonable mechanism for this reaction. Explain why it is exothermic. Н+ Дон H2O

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: Propose a mechanism for the following reaction:

A: A Grignard reagent is an organomagnesium compound which can be described by the chemical formula…

Q: Diazomethane can be used to convert a carboxylic acid to a methyl ester. Propose a mechanism for…

A: Mechanism

Q: What is the major organic product of the following reaction? O HO OH HO O подд ОН sham олгон ОН 0 OH…

A: The objective of the question is to identify the major product.

Q: O ethanal O formaldehyde O epoxide O acetone O carbonic acid QUESTION 4 The reagent/reaction of…

A: Applying concept of organic synthesis and reagent.

Q: What is most likely the first step of this reaction's mechanism? CH CH;CH,OH Br Br CH;CH20- -- CH3…

A: Interpretation-  To tell about which one is the most likely the first step of this reaction…

Q: Propose a mechanism for this reaction. CICH,CH,OH Na,CO, H,0 H,C-CH,

A: Given reaction,

Q: Which of the following compounds reacts slowly during nitration? B OA OC OE B OH C E

A: Nitration of above given compound will takes place with the benzene ring present in the molecule. We…

Q: Treatment of 1,2-dibromoethane with the dithiolate dianion shown in the reaction below leads to two…

A: 1st product C4H8S2

Q: i) НО HO ii) HO OTs iii) суclohexene trans-cyclohexane-1,2-diol O=

A: Please find your solution below : 1. Cyclic esters on reaction with LiAlH4 in presence of ether…

Q: What is the expected product of this reaction scquence? NaC CCH CHCH Br Na THE hgNH (А) CH,CH,CH,с —…

A: In the first step, since CH3CH2Br contains the leaving group, thus the Nu- attacks on the ‘C’ atom…

Q: KI, Oxone H₂O 22 °C, 1 hr Scheme 1: lodolactionization starting materials and reaction conditions OH

A:

Q: Draw the major organic product(s) for the following reaction

A: Since we know that acid react with alcohol to form an ester .  Here , 2 molecules of acetic acid is…

Q: Provide the reagents and mechanism for each step of the synthesis.

A:

Q: Give the major product(s) of the following reaction. H2O, H+ О НО HO OH OH heat OH ?

A: Converting a cyclic ketal to a ketone typically involves hydrolysis under acidic conditions. Here's…

Q: Provide a mechanism for the following reaction:

A: This reaction is the cationic addition polymerization reaction.Here Lewis acid is used as the…