synthesising this molecule with the given reactant

Q: . Draw out all bonds (particularly those to hydrogen atoms) so that you can show the arrow pushing…

A: The branch of chemistry that deals with the structure, properties and the reaction of the organic…

Q: Please correct answer and don't use hend raiting

A: Step 1:

Q: Draw a curved arrow mechanism for the reaction, adding steps as necessary. Be sure to include all…

A: Alcohol (-OH) abstracts proton (H+ ion) from TsOH and tosylate (TsO-) acts as nucleophile in next…

Q: this question. For the following problem, supply all organic products. Include any substitution or…

A: A substitution reaction is a chemical reaction during which one functional group in a chemical…

Q: Which of the following is formed when cyclopentanone reacts with hydroxylamine? "NH2 HO. "NH2

A: "Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Create a Synthetic Route Fill in the missing information that describes how to synthesize the target…

A: Retrosynthesis is the imaginary breaking of bonds present into the molecule into available starting…

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: what are the steps and reagents needed to synthesize this molecule?  only typed solution

A: The required reagent and step involved for this reaction is given below.

Q: Complete the mechanism below by adding curved arrows on the reactant side and drawing the products.…

A:

Q: Needing the reagent, reactant, and/or the product for the following reaction. ||||| ņ LDA DIPA ?

A: LDA is a bulky base so abstract H from less hindered side . For elimination in cyclohexane both H…

Q: Br t-BUOK t-BUOH

A:

Q: 3. Show the mechanism and any intermediates formed in the following reaction. d A

A: retro-Diels-Alder and Diels-alder

Q: Draw the products of the following reactions (Ph)₂CuLi EtOH MgBr EtOH

A: Grignard reagent provides a hard nucleophile and it gives a 1,2-addition reaction with the…

Q: Do not handwriting solution. Thank you!

A: The major organic product of the reaction is (Z)-but-2-ene-2,3-diyldibenzene while methanol and…

Q: Write iupac name Add explaintion each step

A: naming process for each molecule based on its structure:Molecule 1: 3-methylbutyl…

Q: If an acid chloride undergoes an addition reaction with an organometallic reagent, what type of…

A: tertiary alcohol is the correct answer as  if we use organometallic reagent is in excess amount.

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…

A: The mechanism of a reaction shows the electron movements occurring between the reactants during a…

Q: For each equilibrium, circle the side that is present at higher concentration CH3 NH3 NH2 NH₂ NH3…

A: The side which has higher stability will be present in higher concentration.

Q: Fill in the missing information that describes how to synthesize the target molecule from the…

A: Retrosynthesis is the imaginary breaking of bonds present into the molecule into available starting…

Q: Draw the structures of the missing intermediates and products in the following mechanism. Use wedges…

A: The given reaction is a addition reaction.

Q: ند O 1) NaOEt 2) CH₂CH3 3) H3O+

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

Q: What reagents would be used in each reaction (mechanism isnt needed).  State the differences…

A: Aldol condensation reaction is condensation reaction between two aldehydes having alpha hydrogen…

Q: ▷ H- I—Br: Click and drag to start a structure. drawing

A: Given reaction is an example of substitution reaction. In the given reaction first formation of…

Q: draw the step one product and draw curved arrows to show the nucleophilic addition step.

A: To provide the arrow mechanism for the first step of the Fischer esterification reaction and the…

Q: help please answer in text form with proper workings and explanation for each and every part and…

A: The image shows a cyclohexene compound to react with molecular bromine (Br2). This type of reaction…

Q: Predict the major product for this reaction. Ignore inorganic byproducts. 1. BH3-THF 2. H2O2, NaOH a

A: It is an addition reaction in which hydration of unsaturated hydrocarbon alkene or alkyne…

Q: Add the necessary reaction conditions, including any additional reactants needed, above or below the…

A: The objective is to determine the reagent of the given reaction. The transformation of alkene to…

Q: ← Curved arrows are used to illustrate the flow of electrons. Using the provided starting and…

A: This reagent that  is PBr3/DMF  used for conversion of alcohol to alkyl halide .

Q: Please correct answer and don't use hand rating

A: 1: The general reaction can be written as follows: When a ketone is treated with hydrogen gas (H₂)…

Q: For this structure, draw a mechanism that includes all resonance structures for any intermediates on…

A: Given is organic reaction.The given reaction is isomerisation reaction.Due to the presence of…

Q: groups and which of these functional groups will be more reactive to nucleophilic addition

A: Four compounds are given, in which different types of functional groups present. From them we chose…

Q: What major product(s) (from Figure #16) results from the following reaction (from Reaction #16)?…

A:

Q: Could I get help with how to create a three step synthesis problem that starts with an alkane

A: Alkanes belongs to the class of hydrocarbons where all carbons present in the molecule are linked…

Q: Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the…

A:

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.