The following synthesis will no produce the product shown - explain what will happen instead

Q: The major product of the following reaction is он H,SO, heat

A: First lone pair of OH will attack on H of H2SO4. See the written solution.

Q: Predict the MAJOR product by proposing a plausible mechanism. Indicate stereochemistry when…

A: NaH is metal hydride  In presennce of OH group which is higly acidic react with OH and acid-base…

Q: please explain the reaction with mechanism

A: in the given question, it is secondary alkyl halide which reacts with a very good nucleophile. This…

Q: Show how to carry out the synthesis below. Br HO

A:

Q: Shon how you wuld ynthesize to compound below using any reagents. More than one step may be required…

A:

Q: Identify the reagent(s) that can be used to achieve the following transformation: ola. OH O…

A: Oxidation of terminal alkyne to carboxylic acid and carbon dioxide

Q: Ï H CH,CH,NH, The product of the reaction is a semicarbazone. a hydrazone. an oxime. an imine. Q2Q

A: The given question explains the reaction between aldehyde and amine to form corresponding imine as…

Q: Propose a synthesis for each of the following. Show the intermediate step products. If a problem has…

A: The following transformation involves multiple steps.  A. Here, alkyne to alkene followed by…

Q: The following enolate alkylation reaction is attempted in the laboratory as shown: 1. NaOH 2. CH3B.…

A: The given reaction should proceed through the formation of an enolate intermediate followed by SN2…

Q: The following is an aldol condensation reaction which involves two different carbonyl compounds, one…

A: The answer to this question is given below:

Q: NaNH,

A: Terminal alkynes and alkyl halides are used to form substituted alkynes as the product. The base…

Q: Predict the major products of the following base-catalyzed aldol condensations withdehydration.(a)…

A: Given data :  Predict the major products of the following base-catalyzed aldol condensations with…

Q: Using the Wittig reaction, suggest two syntheses of the following product from two different sets of…

A:

Q: Which of the following is the major product of the reaction shown? OH and 01 Oll dilute H₂SO4 سلم لي…

A: In the given reaction first H2SO4 gives hydrogen to carbon carbon double bond to form a carbon…

Q: a) Propose a synthesis route to prepare the following product from the given starting material. Note…

A: The steps involved in the given organic transformation are hydroboration-oxidation, oxidation by…

Q: Please solve by providing synthesis of this reaction, please solve with pictures Not used hend…

A: To do this transformation,at first epoxide react with LiAlH4 , there occurs epoxide ring opening by…

Q: Suggest an efficient synthesis for the following transformation: A The synthesis above can be…

A: 1) E2 elimination reaction 2) Ozonolysis reaction

Q: 10) Synthesize the following compound from any reagents and building blocks 2 carbons or less.

A:

Q: What would be the to the to synthesize Compound from the Starting matenals? given Br hast's FROM…

A: The question is based on the concept of organic reactions. we need to synthesize the product based…

Q: In the box below and starting from anisole (methoxybenzene) and any other necessary reagent propose…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Propose a predict the major product in each of the following reactions

A: Alkene are reactive in nature and undergo addition reaction

Q: An α carbon of a ketone or aldehyde can be alkylated or halogenated under basic conditions. Recall…

A: In the alpha halogenation reaction, an enolate formed from an aldehyde or ketone reacts with a…

Q: For each of the following synthesis, draw the products that would be formed A-D. CI HNO3 H₂SO4 A 1.…

A: The nitration of chlorobenzene gives both ortho and para products. The major product is para Chloro…

Q: В. Propose a mechanism to account for the following reaction. Hint: Start by removing the most…

A:

Q: Predict the major product for the following reaction and provide a stepwise curved arrow mechanism…

A: Benzene ring electron rich due to the π electron cloud. Due to this, they are prone to attack by…

Q: 4) How can you obtain the following compound? H

A:

Q: Draw the structures of compounds A–F in the following synthesis scheme.

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: Q5. Draw the all products and a detailed mechanism for the following reaction? -OCH2CH3 Br CH;CH2OH

A: When any Alkyl halide treated with sodium alkoxide, in Presence of ethanol , elimination Reaction…

Q: The compound below undergoes an intramolecular Aldol condensation reaction to form ONE MAJOR…

A: In aldol reaction when an aldehyde or ketone have alpha Hydrogen reacts with any base it gives α, β-…

Q: Meo Meo Meo, ...H Provide the reagents that would result in the given product.

A:

Q: How would you carry out the following synthesis? CCH3 SO3H

A:

Q: Propose a mechanism for the reaction of benzoic acid with oxalyl chloride. This mechanismbegins like…

A: SOLUTION: Step 1: The best reagents for converting carboxylic acids to acid chlorides are thionyl…

Q: 4. Can the desired product shown below be made by Friedel-Crafts alkylation? AICI3 a) If yes,…

A: Friedel crafts reactions have two types: alkylation and acylation reactions. It is an electrophilic…

Q: Suggest a sequence of reagents that will accomplish the following. MeoloMe HO

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Please outline a synthesis for the following compound under the given restrictions and any other…

A:

Q: Organic Chemistry Problem. Please help with figuring out what steps to take to obtain the product of…

A: Primary alcohols as well as aldehydes such as the given in the problem can undergo oxidation to form…

Q: 8. Provide efficient syntheses for each transformation below. (a) MeO OMe → OMe

A:

Q: Itz Ni Hz Cexcesy Pd

A: Ni and H2 (g)  reduces the alkynes, alkenes, nitriles, dienes, aromatics, aldehyde, ketone, nitro…

Q: 4. Tertiary amines undergo reversible conjugate additions to a ß-unsaturated carbonyls. The reaction…

A:

Q: An aromatic imine is formed when 3,5-dihydroxyphenol is treated with ethanenitrile (CH3CN) in HCI in…

A: In the first step, protonation of ethanenitrile with HCl occurs. Protonation makes the ethanenitrile…

Q: POD4 ropose a synthesis for the following transformation. Include intermediates.

A:

Q: PROVIDE SYNTHESIJ (3STEP)) 에 Thom OH

A: We have been given an organic reaction.The question is based on the concept of organic synthesis. We…

Q: avbe illes Procedu Chemistry 2425: Aldol Condensation H₂C NaOH CH₂ EIOH HOD psbun sittas

A: Well, In the reaction above, by observing the product we can guess, one mole of acetone undergoes…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.