(b) ethanol, HCI соон heat

Q: 1. CH₂CO3H 2.NaOCH3, CH3OH

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: 7. Provide the synthesis for the following product starting with the provide starting material. More…

A: Answer -

Q: Predict all the reaction product(s) and draw the mechanism for each transformation below. Ph Br₂ H₂O

A: Given is organic reaction. Given reaction is halohydrin formation reaction.

Q: 2. By what type of mechanism does the following aromatic substitution reaction proceed? Draw the…

A: The given reaction is an example of  nucleophilic aromatic substitution reaction. The mechanism of…

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: OEt NaBH4 EtOH

A: NaBH4 is a weak reducing agent, so it can only reduce aldehydes and ketones.

Q: Select one deactivator & ortho para director to be on a benzene ring to start.  You will then add a…

A: Ortho- para structure on benzene ring is given as follows -

Q: Provide mechanism and major organic product. 1) NaOCH,CH3' CH;CH2OH 2) H30*

A: Given reaction is interanolecular reaction

Q: Draw the structure of the major product formed by the reaction below. ully HO H₂SO4

A: Given,The reaction is:

Q: Please help me with a drawn mechanism for the shown reaction.

A: Let's draw the mechanism: Step 1: Formation of the Enolate           O                 O(-)…

Q: a. HO Show your work by using only one set of reagents per reaction arrow, and clearly drawing all…

A: The synthesis of the transformation is can be obtained by various reactions

Q: What is the major neutral organic product for the following transformation? ONa ? Major Organic…

A: A base abstracts a proton from the alpha-position of a Carbonyl compound to form an enolate ion.…

Q: Provide a complete, detailed mechanism for the reaction CH;CH,OH shown here.

A: A complete and detailed mechanism for the given reaction can be provided as

Q: Give the mechanism ? он 1. NaBHy meoH 2 H₂O

A: Note : NaBH4 is used to reduce keto to alcohol. Acid FG reacts will not react with NaBH4. ( For…

Q: Show the formation of given product with mechanism.

A: Ethylene glycol is generally use for protection of ketone. Hydrolysis reaction in acid medium used…

Q: There are two possible products for the following reaction. Draw both. OH K₂Cr₂O7 H₂SO4

A: The given reaction is an example of oxidation reaction.In this reaction potassium dichromate(…

Q: Complete a mechanism for the given reaction.

A: In the above reaction, we have reactant 2 with carboxylic acid and alcohol functional group. Hence…

Q: Give the reagents necessary for the synthesis above and please show the detailed step-by-step…

A: The reactant is Ethyl acetoacetate. The reactant contains the methylene protons which are highly…

Q: ОН Д CO₂H H2O да

A: Alcohols participate in dehydrationTertiary Alcohols readily participate than the primary and…

Q: Consider the reaction scheme shown below. HCI [1] HO. (a) Provide a detailed mechanism for reaction…

A: This reaction will occur via 3 step. In first step protonation then Water molecule eliminate to…

Q: draw a dehydration reaction and provide a detailed mechanism, explaining the formation of all…

A: In chemistry, a dehydration reaction is a type of chemical reaction where the loss of water takes…

Q: хон HI

A: Alcohol + HI -----> Alkyl halide

Q: 1. The following reaction is performed under basic conditions. Draw the product and show the…

A: Interpretation- As given here the SN2 reaction is an example of a nucleophilic substitution…

Q: Please show me the retrosynthesis and synthesis with detail steps.

A: To get the starting material we have to do the retrosynthetic analysis by doing this we get, 2-…

Q: Give a clear handwritten answer with explanation needed...complete the given reactions with missing…

A: Cyclic ketone undergoes alpha alkylation by treating with base and alkyl halides. The alpha-beta…

Q: provide synthesis for this reaction including all reagents and mechanisms with steps ↑

A: This can be done like this

Q: the question is: which of the following is (SN1, SN2, E1, E2 )? The product C is: The product D is:…

A: NaOH  acts as a strong base  prefer to do elimination rather than substitution .  Sodium…

Q: CI ***** A Et Et Et B Et C Et Et D

A: ->In E2 elimination reaction antiperiplanar beta hydrogen eliminated and alkene formed.

Q: Show the full reaction mechanism and include its name

A:

Q: Draw a complete, detailed mechanism for the following reaction and predict the product(s). CH,OH ?…

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

Q: Oxidation-reduction in two different ways, using appropriate reagents and reactions with…

A: Benzaldehyde oxidation reaction = Conversion of benzaldehyde to benzoic acid

Q: + HO Br

A:

Q: 1. Give the mechanism. 我些我

A:

Q: What reagents would you use to give the product shown below? Show the full mechanism. ? OH

A: The question is based on the concept of organic reactions. we need to identify the reactant required…

Q: e Tson t

A:

Q: но-н HOⓇ OH

A:

Q: Complete the following reaction:

A: Alkene gives hydration reactions in the presence of an acid catalyst. The reaction follows an…

Q: Give the complete detailed mechanism for the following reaction

A: In the given reaction the acid chloride reacts with methoxide ions to form an ester, by nucleophilic…

Q: Identify the major product. X Heat ?

A: Pericyclic reactions are those which can take place in presence of light or sunlight. These…

Q: PPh,

A: When triphenyl phosphine reacts with aldehyde molecule, after rearrangement mechanism, it produces…

Q: gh+lazad

A:

Q: Provide mechanism to get the product

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Choose the best reagents to complete the reaction shown below.

A:

Q: Give detailed Solution with explanation needed..don't give Handwritten answer

A: Hydration of alkyne is the addition of water molecules to the alkyne in presence of sulfuric acid to…

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.