Give the major organic product(s) of the following reaction. 1) H2C=CHM9BR 2) H30*

Q: Given the following reaction sequence: What are the reagents for reaction 7? A) HBr 2 eq B) Br2

A: Given  Find out the reagent for reaction 7

Q: 4. Provide the reagents (at the reaction arrows, use 1).... 2).... if more than one step is needed)…

A: 1) First reaction is haloform reaction. Addition of dihalogen to methyl ketone in presence of base…

Q: 14. Draw the two reactants used to form the following compound, label the nucleophile and the…

A: According to guidelines i can answer only first question. Please repost the other questions.

Q: 1. TsCl.pyridine CH,OH 2. CH,CH,CH,S-

A: Step 1 :  In the first step of reaction alcohol is activated by being converted into sulphonate…

Q: What is the major product obtained from the reaction of 2-ethyloxirane with each of the following…

A: (a) In the presence of acid catalyst, this reaction takes place through partial SN1 and partial SN2…

Q: Preamble: A reaction flask contains a 2-bromopentane in an ethanolic solution of sodium ethoxide at…

A: The products that would be formed from such a reaction have to be predicted. The reaction pathway is…

Q: Hydroylsis of 4-chloro-2-methyl-2-pentene gives two isomeric substitution products, one of which is…

A: In hydrolysis reaction of an alkyl halide , the group is nucleophilically substituted by -OH group.…

Q: 32. Which of these generic structures denotes a ketone? E. I RCH F. I RCOH C. R-O-R' D. R-NH-R' G.…

A: A- R-Cl = Haloalkane B- R-OH = alcohol C- R-O-R' = ether D- R-NH-R' = secondary amine E - RC=O(H) =…

Q: QUESTION 1 Which of the following alkynes will form only 1 product in an acid-catalyzed hydration?…

A: 1. 1-hexyne is a terminal alkyne. Hence, it will give single product in acid catalysed hydration.…

Q: What product results from the reaction of acetone, CH3C(0)CH3, with methylmagnesium bromide and…

A: We'll answer first question as the question to be answered is not specified. Please resubmit the…

Q: What is the product of the HALOHYDRIN below DISREGARD THAT IT SAYS Hydrohalogenation on top of the…

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Q: 2) identify the starting materials, reagents, or products for the following reactions. SOCI, /…

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Q: B. Why are the following conversions poor synthetic methods to prepare the desired products? + N2OH…

A: Answer is explained below.

Q: Select the reagents you would use to synthesize the compounds below from benzene. Use the min List…

A: The question is based on the concept of chemical reactions. we have been given reactant and…

Q: Preamble: A reaction flask contains a 2-bromopentane in an ethanolic solution of sodium ethoxide at…

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Q: Provide a mechanism for the following reaction. Show each step in your mechanism and use curved…

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Q: 1. For each of the following compounds, give a name or draw a structure, as appropriate.…

A: IUPAC rules for naming an organic compound: 1. Select the longest possible continuous carbon chain…

Q: 31. Which of the follow ing is the correct name for the structure below? а. trans-4-nonyne c.…

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Q: Q10:- Explain how Esters are more reactive than amides in nucleophilic acyl substitution reactions.

A: The structure of ester and amide are as follows:

Q: Which of the following reagents would be used to convert 1-pentene to 1, 2- dibromopentane? O…

A: Here, we have to find the reagent that is required to convert 1-pentene to 1,2-dibromopentane.

Q: The reaction of 2-methylpropene with HBr in ether is described below. Answer the following questions…

A: Given reaction is :  Which product is the anti-Markovnikov product = ?

Q: Identify the product in the following reaction. i , KOH ? ii pyrrolidine , heat

A: We have given the organic reaction and we have to find the major product of the reaction.

Q: Esterification reactions, such as the one below, is a poor synthetic strategy as it leads to poor…

A: Carboxylic acid reacts with alcohol in the presence of an acid catalyst to form an ester, the…

Q: How are the following conversions carried out?(i) Benzyl chloride to benzyl alcohol,(ii) Methyl…

A: (i) Benzyl chloride can be converted to benzyl alcohol on the reaction with aqueous potassium…

Q: KMNO4

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Q: + HCI (1 mole)

A: The mechanism of the reaction favours the formation of a stable carbocation. A tertiary carbocation…

Q: Given the criteria for the starting substrate, show the reaction you would use to efficiently…

A: a ) Here we will use HBr peroxide as a reagent  to convert alkene to haloalkane . HBr peroxide is…

Q: Ho ОН НО H20

A: HSAB stands for hard and soft acids and base. According to HSAB principle, hard acids bind…

Q: Which major product is formed when Br2 and H20 are added to 2-methylpropene to give the bromohydrin?…

A: When Br2 and H2o are added to 2-methylpropene, it gives the bromohydrin.The mechanism of bromohydrin…

Q: A 人。 OCH3 H2SO4 он CH;OH

A:

Q: What is the predicted product of the reaction shown? 1. DMSO, (COCI)2… 1-hexanol 2. EtzN

A: 1. This is an swern oxidation reaction.  2. Here alcohol ic converted into ketone or aldehyde.  3.…

Q: Preamble: A reaction flask contains a 2-bromopentane in an ethanolic solution of sodium ethoxide at…

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

Q: 20) Reduction of a ketone with NaBH4 will result in the formation of A) a primary alcohol B) an…

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Q: Starting with an alkyl halide, how could the following compounds be prepared? a. 2-methoxybutane b.…

A: Please find below the reactions

Q: 25. What is the major organic product of the following reaction? 1. O, -73C ECH-CH3 2. H,02

A:

Q: What is the major product obtained from the reaction of 2-ethyloxirane with each of the following…

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

Q: 4a. Which type of molecule is this? Label the nonpolar and polar regions of this molecule. Label the…

A: Lipids are triglycerides are formed from fatty acids and glycerol.

Q: Preamble: A reaction flask contains a 2-bromopentane in an ethanolic solution of sodium ethoxide at…

A: Given reaction,

Q: N. NH2 NaOH H,0, A

A: We have hydrolysis of the amide with the base catalysis ,we have to draw mechanism for this .

Q: unu=de QUESTION 32 Which one of the following types of compounds is the most reactive in…

A: The rate of nucleophillic acyl substitution depends upon the leaving group tendency.

Q: Draw the organic product(s) of the following reaction. 1. K2CO3 H. 2. distill

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Q: Ozonation followed by oxidative workup of an alkene gave the following products. What was the…

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Q: 6. For the following reactions, draw and name the products. If there is no reaction, simply put NR.…

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Q: (a) Give the reagents that are used to form the following products. R R Alkenes он R- R' |(D)…

A: A) Alcohols to alkyl halides- Treating alcohols with Halogen acids leads to the formation of alkyl…

Q: 1) Which of the following the alkyl halides reacts the fastest in an SN2 reaction? * A.…

A: Nucleophilic substitution is the displacement of a leaving group by a nucleophile. A nucleophile is…

Q: 11. The molecule below is reacted with ethylene glycol in acidic conditions. The product contains…

A: The solution of the given question is

Q: Draw the organic product(s) of the following reaction. OH но-он p-toluenesulfonic acid benzene, 80º

A: This  is basic reaction of protection of ketone. Here, using ethylene-diol in presence of diol we…

Q: In Experiment 66: An Oxidation Puzzle, one alcohol on the starting material was selectively oxidized…

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Q: What is the major organic product obtained from the following sequence of reactions? Mg H20 Br Et,0…

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Q: Provide the reagents necessary to complete the following reactions. More than one step may be…

A: Here we have to convert 1-bromo-2-methylpropane to 1-propylcyclohexan-1-ol by multistep reactions.

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.