H3CO. 1. NaOCH3 2. H20 OCH3

Q: Which bases can be used for an E2 reaction that follows Hofmann's rule? Choose all that apply. O…

A: According to Hoffman rule, an elimination reaction occurs to produce less substituted alkene which…

Q: OH 1. LIAIH4, THF OCH2CH3 2. H3O* HOCH,CH3

A:

Q: Draw the product of attached reaction ?

A: In the reaction, following steps will take place. 1) The alkene given (not benzene) will take proton…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. CI H2O pyridine

A: The chemical reaction given is

Q: BOH)2 Pd(PPH3)4 Br K2CO3

A:

Q: Draw the product of attached reaction ?

A: When R-SH reacts with bromine, it gets oxidized to disulfide. The hydrogen atoms from both the thiol…

Q: Please draw the stepwise mechanism for this reaction !!

A: Concept based on organic chemistry reaction mechanism.

Q: Which reacts faster in an E1 reaction?

A: A weak base is favoured E1 reaction because carbonation is the intermediate in that reaction which…

Q: Vill the following bases favor an E1 or E2 mechanism? Sort them into the appropriate boxes below.…

A:

Q: Draw the final organic product for this reaction: NaOH

A:

Q: 2. Draw a stepwise mechanism for the following reaction. Use curved arrows to show electron flow.…

A: Deprotonation of Acetals:

Q: H HCI

A: Welcome to bartleby !

Q: Draw the products of attached nucleophilic substitution reaction.

A: The products of attached nucleophilic substitution reaction can be drawn as,

Q: Need help with this SN2 esterification reaction mechanism with pushing arrows. Please help.

A:

Q: + en

A:

Q: Draw the product of attached reaction.

A: The mechanism is as shown below:

Q: Give one example of Williamson ether synthesis. Show the reactants materials and the product. Draw…

A: As per the multiple-question rule- I am answering the first question asked (Williamson-ether…

Q: Provide the synthetic route for the following reaction?  (CH3)2CHCH2Br ----> (CH3)2CHCH2CH2CH2NH2

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. CI 2 eq H20 +

A:

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

A: In the given reaction benzaldehyde react with methyl amine.

Q: но. PhHNNH2 NHPH 'N' -Me H30*, pH 5 OH

A: Applying concept of reagents and chemical reaction.

Q: out of each pair which undergoes a faster E2 reaction

A:

Q: Draw a mechanism for the following reaction. Highlight the intermediate formed at the end of step 1,…

A:

Q: Use a curved arrow to show the nucleophilic attack. Select Draw Rings More Erase cHO H H-Ó: :0H H H…

A:

Q: What major product (from Figure #1) results from the following dehydration reaction (from Reaction…

A: Alcohol gives dehydration reactions when they react with a strong acid like H2SO4 or H3PO4 to form…

Q: i. O3, ii. PPh3 CH2CI2 H

A: The mechanism is as follows:

Q: This reaction can be completed with which reagents?

A:

Q: For C, D and E, determine which step undergo the elimination, substitution or additor State the…

A: Given : We have to choose reagents for each step.

Q: Draw the products in attached reaction?

A: The products in the attached reaction should be drawn.

Q: Show a mechanism with curved arrows for the reaction.

A: The given reaction is,

Q: Draw curved fishhook arrows to show the movement of electrons in this step of the reaction…

A: In a free radical reaction mechanism, the homolytic bond cleavage takes place. During homolytic bond…

Q: write complete mechanism for reaction. show electron pushing arrows.

A: The reaction of alkene with halogen in presence of water, produces halohydrin.

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

A: The reaction given is,

Q: acid anhydride alcohol

A:

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

A:

Q: . Complete the proper curved arrow mechanism for the reaction shown below. Br H-Br

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: NH2 NH2 TCI AICI3 aniline

A:

Q: Draw the major product of this reaction. Ignore inorganic byproducts. HO, 1. SOCI2 2. CH3CH2OH,…

A: Given reaction: We have to find the major product of this reaction.

Q: KOH, CH3CH2OH reflux Please sele Draw Michael Adduct KOH, CH3CH2OH reflux Draw Robinson Product

A: Given ; structure of reactant.

Q: Draw the products of attached reaction using the two-part strategy

A: This problem deals with reaction of an alkene with a protic acid, here the acid is HBr, so the…

Q: OH но OH BF3'Et20 HO HO `OH

A: Alcohol react with lewis acid and carbon attached to -OH becomes more electrophillic which further…

Q: Draw a stepwise mechanism for the attached reaction.

A: Given reaction,

Q: Carefully draw the mechanism of the following reaction using arrows to show the movement of…

A: The given reaction is an example of Electrophilic Bromination of Benzene.   This reaction occurs in…

Q: Draw the Wittig reaction mechanism with arrow pushing.

A: Wittig reactions are helpful in alkene synthesis using aldehyde/ketones on treating with triphenyl…

Q: Draw the product of the attached reaction:

A: In this reaction, OH- acts like base and it abstract the more acidic hydrogen and then negative…

Q: OH

A:

Q: H2SO4 +

A: The reaction taking place is given as,

Q: Provide a curved arrow mechanism for the SN1 reaction below: CI CH3 H,C NACN

A: SN1 is a unimolecular nucleophilic substitution reaction. A carbocation is formed after the eviction…

Q: What reaction is occurring? Circle one. 1. LIAIH4. -ОН Nucleophilic Substitution Reduction 2. H20…

A: Since LiAlH4 is an strong reducing agent as it produces H- ions in the solution. Hence it reduces…

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.