The following reaction does not produce the desired product but does produce a product that is a constitutional isomer of the desired product. Draw the product that is obtained and propose a mechanism for its formation: OH OH 1) NaNH, 2) MeI 09.70a Modify the given structure to draw the product of this reaction. Do not use abbreviations when drawing the product. OH CH Edit Drawing

Q: select the major 1. NaOCH2CH3 CH3CH2OH CH3CH30 OCH2CH3 2. H3o+ OCH2CHS OCH2CH

A: The given reaction is an example of an intramolecular Claisen condensation reaction.

Q: 3. For the following two reactions (a) Draw all possible products (b) For Reaction 1, propose a…

A: The question is based on organic reactions. We need to identify the product and explain its…

Q: ONa HO но NOT FORMED HO HO

A: Note: Phenol reaction with t-BuOK give phenoxide ion. This phenoxide removes beta proton of alkyl…

Q: The following reaction does not produce the desired product but does produce a product that is a…

A:

Q: Draw the alcohol that is formed when the following alkoxide ion is treated with H3O+, and show a…

A: In the given question,  an alkoxide ion is given and we have to find the alcohol formed when it is…

Q: Can you do it and explain it in detail? Show the mechanism

A:

Q: 9. Which rule states tha that proceeds via the A) O'Doyle's Ru B) Markovnikov C) Zaitsev's Rul D)…

A:

Q: NaOH 12 excess

A: The given reaction is a haloform reaction where methyl ketone reacts with iodine, bromine or…

Q: After running various experiments, you determine that the mechanism for the following reaction…

A:

Q: .N. NH2 HO. CF3 CF3

A: The given incorrect reaction is :  Draw the mechanism with this new reactant(s) to obtain the…

Q: Predict the product and draw the mechanism of its formation. Include lone pairs and charges in your…

A: Answer given as follows

Q: For the following reaction, predict the major product and draw a mechanism for its formation. Me HBr…

A: The epoxide ring can be opened by its reaction with HX, where X is a hydrogen halide. This reaction…

Q: Predict the elimination products for the reaction. Identify the major and minor stereoisomers and…

A:

Q: OH Br 3. Br pcc I) CH3 myBr 2)H30+ OH

A: PCC(Pyridiniumchlorochromate) is an oxidizing agent that oxidises secondary alcohol  into ketone.…

Q: To propose an intermediate and mechanism for the transformations

A:

Q: Suppose this reaction happens by the SN 1 mechanism: хоч Br но

A: SN1 Mechanism is followed in two steps - A stable carbocation is generated by removal of the leaving…

Q: Draw the mechanism for the acid-catalyzed reaction of acetic acid (ethanoic acid) with the methanol…

A: The given reaction is an good example of formation of an ester from its corresponding carboxylic and…

Q: None

A: Step 1:Here is the step  1 mechanism and the intermediate product  Computer typed version:

Q: What is the major product of the following multi-step synthesis? 1. BH3 2. H₂O2, NaOH HBr HS. t + &…

A: Hydroboration-Oxidation reaction is a chemical reaction…

Q: Draw the structure of the major organic product of the following reaction. Predict whether the…

A: The given reaction is Aldol reaction. In this reaction when two moiety of aldehyde or ketone (…

Q: Which reaction will produce a monohalogenated alk halide? Select the correct response: O…

A:

Q: Following reaction takes place in one step2NO + O2→ 2NO2 How will the rate of the reaction of the…

A: the rate law of a chemical reaction guides about the relation of rate of reaction and concentration…

Q: Draw the correct structure of the indicated product for each reaction. `Br KCN H,O+ product 1…

A:

Q: Alcohols OH OH

A: Since you have multiple questions, we will solve only first question for you. In order to get other…

Q: The reaction of 2,2-dimethyl-1-propanol with HBr is very slow and forms 2-bromo-2-methylbutane as…

A:

Q: Draw an alkyl halide and choose the best reaction conditions that would undergo an SN2 reaction to…

A: Alkyl iodide reacts with alkoxide ions to form an ether.

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

A:

Q: What is Henry’s law? For what kinds of calculations is Henry’s law useful?

A: According to Henry’s law, the solubility of a gas is directly proportional to the partial pressure…

Q: Draw the products of the two step reaction sequence shown below. Ignore inorganic byproducts. If the…

A: When the benzene reacts with an alkyl halide in the presence of a Lewis acid catalyst alkyl benzene…

Q: A student draws the mechanism for a carboxylic acid deprotonation. All three arrows are incorrectly…

A: A student has drawn a wrong mechanism for a given reaction. Redraw the mechanism correctly.

Q: Be sure to answer all parts. Draw the products in the following reaction. of CH,CH,OH Part 1 out of…

A: Organic reaction mechanisms

Q: Br Br 1) 3 NaNH, 2) Butanone 3) H3O+

A:

Q: (h) CH, CO CH,CO,H, 50 Draw the major product(s) of the reaction. H₂C CH3 Edit Drawing Draw the…

A: In this question, we will draw the structure of major and minor products. Substitution product is…

Q: Draw the products that are expected for the following reaction. q Modify the given structure of the…

A:

Q: A synthesis of the anti-tumor agent tamoxifen is shown below. In the following questions, you will…

A: Given is organic synthesis scheme.The given scheme is for anti-tumor agent tamoxifen.

Q: Although we often show protons that evolve in chemical processes by using the notation H+, "free"…

A: Since you have asked multiple fill in the blank questions, we are answering the first three for you.…

Q: охсхо 11 III F NV + : -CH₂ (X) -CH₂ н, с CH₂ CH₂ I P S F CI Br 0 Т с N

A:

Q: Draw the structure of the major organic product(s) for the following reaction between an acetylenic…

A: Given reaction is nucleophilic substitution reaction.

Q: Draw an arrow-pushing mechanism and identify the product(s) for each reaction below and specify the…

A:

Q: A student proposes the following mechanism for a nucleophilic substitution reaction: Br: ? Notice…

A: The bimolecular nucleophilic substitution reaction is a concerted reaction that occurs in a single…

Q: Propose a mechanism for the chemical reaction below. Which step in your mechanism is…

A: Given : reaction

Q: H H CH3 H;C CH3 H;C CH3 CH3

A: Protonation of alkene Carbocation rearrangement (formation of more stable carbocation intermediate)…

Q: 15. Write is the products of the following reaction? DRAW the mechanism for this reaction. H+…

A: Given reaction is substitution reaction in whichH is replaced by tert -butylbenzene.

Q: HBr Br HO 65°C

A: Protonation of alcoholic oxygen  Loss of water molecule as a leaving group  Carbocation…

Q: OH NO₂ 10 pyrrolidine 7 (4 equiv) paraformaldehyde 8 (4.5 equiv) 100 °C, 4 h, neat OH N NO₂ 11 (not…

A: Here we have to write mechanism of the following reaction.

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.