NaCN Dimethylformamide

Q: Which statement best describes what is happening in step 6? (Remember, this is copied from the full…

A: In the given step left side one is imine. Imine is converted to examine  through tautomerisation

Q: Please help me find the reagents of the synthesis

A: To solve this problem we have to do following steps (1) alkyne is treated with NaNH2 to form a ionic…

Q: `OH

A: In given reaction   , alkene is converted into alcohol.

Q: ow the starting materials you would use in the Heck reaction in order to create target molecule…

A: Heck reaction is palladium coupling reaction, of aryl or vinyl halide with alkene .

Q: In order to complete the synthesis shown below, you would need to use [ Select ] as the nucleophile…

A: SN1 reactions are favoured by the attack of nucleophile from the same direction as that of the…

Q: NH2

A: For this transformation,  SHAPIRO Reduction is used . Here the the concept of umpolung or the…

Q: O CH3CCH₂CH₂CH3 NaBH4/CH3OH

A: NaBH4 acts as a reducing agent by providing H- ion . It reduces Aldehyde into a primary alcohol and…

Q: Perform a retrosynthetic analysis of the following target and come up with the synthetic route. OEt…

A: There are number of functional group associated with organic compounds which impart specific…

Q: CCHCH3 CH30 H3CH2C е. CH2CH3 CH3OH

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Q: Please provide a way to synthesize the target compound using the reagents given below once Target…

A: The conversion reaction is given in the following step.

Q: What is the final product of the following reaction sequence? Give structural details of all…

A: 1) Removal of most acidic H by NaH.

Q: Please help ASAP Provide the reagents or sequence needed to convert p-methylbenzaldehyde to each of…

A: We have find out the reagents for conversion.

Q: Please provide a mechanism with curved arrows by replacing MgBr with 3-methoxyphenylmagnesium…

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Q: The process shown below, the conversion of the electrophilic benzylbromide (1) to a nucleophilic…

A: The process shown below, the conversion of the elecrophilic benzyl bromide (1) to nucleophillic…

Q: Alkyl diazonium salts (shown below) are considered "super" leaving groups; a consequence of this is…

A: Alkyl diazonium salts are the excellent leaving group because R- N2+ because nitrogen is an…

Q: This will require more than one step of reagents to arrive at the final product. Write the…

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Q: NaOEt ELOH, heat

A: -> NaOEt is base which can abstract most acidic hydrogen and generate nucleophile. ->Then…

Q: Br2 / N2OH R-CO-NH2 R-NH2 H20

A:

Q: This is the reaction I was referring to, I have no idea of what reagents can lead me to the…

A: In this reaction, the reagents are H2O and KMnO4.

Q: please help me to make synthesis of chrysin (5,7-dihydroxyflavone) in 4 or more steps and start for…

A: Chrysin is a dihydroxyflavon in which the two hydroxy groups are located at positions 5 and 7. It…

Q: Choose the reagent(s) that would be most likely to complete this reaction. Br

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Q: Using the Strecker Reaction, please show the steps and the final product of the following reaction:

A: Strecker synthesis is preparation of alpha- aminonitriles which are intermediate for the synthesis…

Q: Starting with 3,5-hexadiyn-1-ol, select reagents from the table below that should be used to…

A: The reagents are faigb i) protection with TBDMS-Cl ii) deprotonation of terminal alkynes iii)…

Q: Show the product and arrow pushing mechanism for the following reaction. Make sure that label the…

A: The product of the given organic reaction is as follows.

Q: Draw the product of the given reaction sequence. Select NaOCH3, CH;OH

A: Robinson annulation combines a ketone and an (alpha, beta) unsaturated ketone. The reactions are…

Q: Name the major and minor products for an SN1 reaction with iodide for the following compound:

A: In the SN1 mecanism first carbocation form and then nucleophile will attack.

Q: In each reaction box, place the best reagent and conditions from the list.

A: Cyclohexanone on reaction with Br2/NaOH gives 2-bromo cyclohexanone. This on treatment with…

Q: Please finish this mechanism problem and show all movement of electrons and any thing you used to…

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Q: Select the major organic product of the reaction. NaBH4, MEOH product

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Q: 1. Examine the given reaction below. This is a intramolecular Friedel Crafts acylation reaction. As…

A: A question based on Friedal-Craft acylation reaction, which is to be accomplished.

Q: 2. Answer ALL parts. a) Write a detailed reaction mechanism for the following conversion. он Acetone…

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

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

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Q: Draw a detailed mechanism for the chlorination of benzene using Cl2 and FeCl3.

A: The general reaction is as follows,

Q: а.) b.) с.)

A: Acetals on hydrolysis gives corresponding aldehyde or ketone and alcohols. Let's see here,

Q: Which compound is a major product of the reaction sequence shown in the box? 1. EtO Na+ OEt 2. HСI,…

A:

Q: For SN1 Explain if 3o ( tertiary) alkyl halides reacted (fastest or slowest) explain why. Be sure…

A: In unimolecular nucleophilic substitution reaction, the intermediate formed is carbocation. More…

Q: QUESTIONS 1. Examine the given reaction below. This is a intramolecular Friedel Crafts acylation…

A:

Q: Na HO, Br

A: When an alcohol is treated with NaOH, the following acid-base equilibrium occurs.   The…

Q: Who would compound X be in the following sequence of reactions? Select one:

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Q: 1. CgH5MgBr then H30* 2. H3PO4, A 3. Оз. На02

A:

Q: Please show me the mechanism for O3+2-methyl-2-butene, stoping at the ozonide?

A: Ozonolysis is an organic reaction in which ozone is reacting with unsaturated compounds such as…

Q: 2. Draw out the forward synthesis (fill in the boxes) only for the following transformation (it'll…

A: Here we have to make a desired forward synthesis for below conversion .

Q: OH3C HCO- 1 hoi H 2 1) C4HgLi 2) THF OH3C ΗΤΗ H OIS H 3

A:

Q: 2. Answer ALL parts. a) Write a detailed reaction mechanism for the following conversion. ОН HO…

A: We have to give the mechanism of the given reaction.

Q: 3-) Show the mechanism by using curved arrows for the reaction between following lactone and…

A: Question a compound of lactone is a reaction of ethyl magnesium bromide and H3O+ can be mechanism is…

Q: NO2

A: The organic reaction takes place in many steps. These steps involve the use of various reagents.

Q: H₂O /H₂SO4 HgSO4 NaBH4/CH3OH

A: Given reaction is :  Predict the products of the reaction ?  According to Markovnikov's rule,…

Q: benzaldehyde 9 H ethyl formate -OCH₂CH3 1. pyrolidine O 2. 3. H₂O* 8 10 ya ii + excess benzaldehyde…

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

Alkynes

Alkynes are organic compounds that contain at least one triple bond between carbon-carbon atoms. They are a series of unsaturated compounds with a general molecular formula, CnH2n-2.