[1] NaCN Br [2] LIAIH, [3] H2O

Q: Draw the products of each reaction.

A: As you have posted multiple subparts in 1 question and have not mentioned which part you want us to…

Q: Draw the mjor product of both question with mechanism asap

A: Given structure of reactants.

Q: Draw a stepwise, detailed mechanism for attached reaction.

A: A detailed mechanism for the given reaction can be drawn as,

Q: Draw any product of dehydrohalogenation ?

A: The type of elimination reaction in which a hydrogen halide is removed or lost from the reactant is…

Q: Ho,

A:

Q: at product will result from the reaction shown? (Just mention the class of compound not the…

A:

Q: Select the electrophile (A, B, or C) in the following reaction step.

A: Electrophile is an electron deficient species or a neutral compound having an incomplete octet or…

Q: Draw the products of attached reaction by following the curved arrows.

A: The products of attached reaction can be drawn as

Q: Bonus: What anion is a more reactive nucleophile? Why? Must draw a picture! VS.

A:

Q: Br2 CH3OH

A: Organic reaction mechanisms

Q: mechanism and draw the product

A:

Q: Draw the product of attached reaction.

A: The mechanism is as shown below:

Q: Which EAS reaction is matched with the WRONG electrophile

A: We have been asked which electrophile is wrong for particular Reaction in electrophile aromatic…

Q: Draw all the products of the following reaction:

A: Please find below all the possible products of the above reaction.

Q: Draw the PRODUCTS of the reaction and draw the COMPLETE MECHANISM of the reaction.

A:

Q: AICI,

A: Friedel-Crafts alkylation is an alkylation of aromatics using an alkyl halide and a Lewis acid…

Q: Draw the major product(s) for:

A: Aldol condensation uses an enol or an enolate to react with a carbonyl compound to form…

Q: Draw the product of attached reaction ?

A:

Q: Draw a stepwise detailed mechanism that illustrates how four organicproducts are formed in the…

A: Substitution reaction: When one functional group of a compound replaces the other functional group,…

Q: or each addition route of the reaction, draw the structure(s) of the major product(s), including…

A: Answer of the question given below,

Q: NaH

A: Aldol condensation : In presence of base when ketones or aldehyde reacts to another keto or aldehyde…

Q: Draw the missing curved arrow notation to incidate how the carbocation in left box rearranges to the…

A:

Q: Draw the products of attached reaction, and indicate the stereochemistry where appropriate.

A:

Q: Draw ths missing curved arrow notation for the E2 reaction. AV

A: The secondary and tertiary alkyl halides proceed with E2 mechanism in the presence of base HO- .…

Q: Draw all possible products in the following reaction and circle the most stable product. Br КОН ELOH

A: In this question, we will draw all products for this reaction and the circle the most stable…

Q: Draw the products of each reaction

A:

Q: НО. HI

A:

Q: Draw the products of attached reaction by following the curved arrows.

A: The product of attached reaction is determined as shown below,

Q: What reagentls) will perform the following miction?

A: The given reagent is a ketone. It belongs to the carbonyl family. the IUPAC name of the compound is…

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

A: Interpretation: The products of attached reaction using the two part strategy to be drawn.

Q: Draw the products of the reaction and rank the reactions from fastest to slowest.

A: Nucleophilic reactions are those reactions in which a nucleophile attacks the carbon of carbonyl…

Q: d provide all the necessary reagents in class and any reagent

A: In Organic synthesis the reactant is converted into desired product using specific reagent

Q: ne major product?

A:

Q: 2. Draw the complete, detailed El mechanism for the following reaction (including including curved…

A: Tertiary alkyl halide gives E1 elimination to form an alkene. The alkyl halide eliminates hydrogen…

Q: Figure can potentially react as an electrophile or as a nucleophile in different chemical reactions?…

A:

Q: 4.2 Draw the product(s) of the following reaction by following the curved arrows.

A: Given incomplete reaction is : Draw the products of the reaction by following the curved arrows = ?…

Q: DA. One product is formed, and it is achiral.

A: A carbon center which is sp3 hybridized and is bonded to four different atoms is called chiral. NaH…

Q: what is the structure of A in the given reaction map?

A: Given reaction:

Q: Draw the mechanism for the following reaction. H.

A:

Q: Friefly explain why the following synthetic step is incorrect, and rewrite it so that it is correct.…

A: Need to correct the product for the given reactant.

Q: Draw the major product of this reaction. Ignore inorganic byproducts. H3O*, heat P Type here to…

A:

Q: In the electrophilic addition step shown here, where NO, adds to phenol, the electrophile can add…

A:

Q: Please label any nucleophilic centers or electrophilic centers.

A: The nucleophilic center is the electron-rich center. The electrophilic center is the…

Q: Draw the products of attached nucleophilic substitution reaction.

A: In nucleophilic substitution reaction the leaving group is replaced by the electron rich species…

Q: soogain aftex gepeatation this single -H š heplacad by -OH

A:

Q: Question attached

A: E2 elimination or bimolecular elimination as the rate of reaction depends on the concentration of…

Q: Draw the products of attached reaction by following the curved arrows.

A: The products of attached reaction by given the curved arrows can be drawn as

Q: Draw the product of attached reaction ?

A: GIven,

Q: What’s the stronger nucleophile in each pair?

A: How to decide strong nucleophile ( strong base). Step 1 : take conjugate acid of the base. Assign…

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.