8) Consider the below desired transformation. Develop a retrosynthesis and forward synthesis that would successfully accomplish it. -

Q: O Propose a retrosynthesis and then a synthesis for the transformation below. oh HO

A: Given is organic synthesis reaction.In this reaction reactant is Carboxylic acid and product is…

Q: O2N. НО НО- OH

A: Applying concept of organic synthesis and reagent.

Q: NO2 Br

A: The conversion is given below in pic.

Q: O

A: Base deprotonates the most acidic proton of cyclodiketone compound and inducible carbanion acts as…

Q: One example of an eleven carbon terpene is shown below.  Draw a curved arrow mechanism showing a…

A: In this question, we want to draw all intermidiate and curved arrows in the mechanism.  You can see…

Q: Please show retrosynthesis and synthesis.

A: The given target molecule is We have to draw both the retro-synthesis and Synthesis reaction.

Q: Identify compounds A-M in the following reaction sequence.

A: Given,

Q: Gabriel synthesis

A: Reaction of potassium phthalimide with haloalkanes or  with other alkylating agents leads to the…

Q: Br Br,, Target Molecule

A: Retrosynthesis is a technique used to analyze the target molecule to identify the starting…

Q: NO2 Он ? ? -CH,CH2OH

A:

Q: Which reaction sequence would accomplish this transformation? OCH2CH3 HO (A) NaH Å CH;CH,I_ (B)…

A: In order to carry out the given conversion reaction, we have to consider the given options and…

Q: renurasize the following molecules from the given starting materials as your only carbon sources…

A: Bromination of alkane using Br2/ light or NBS/ light occurs via radical mechanism through the…

Q: Draw all stereoisomers formed in the following two-step reaction sequence.

A: mCPBA is meta-chloroperoxybenzoic acid is widely used as an oxidant in organic chemistry.  mCPBA…

Q: `CI "OH NO2 ÑO2 C OH R. MgBr .R' R. 1. R' `R' 'R' ОН 1. OsO4 2. H2О2, Н2О ОН ОН E A HCI H2O ОН

A: The given reaction is represented as follows:

Q: Provide a synthesis for the attached problem

A: Needed compound is an alkene, in general elimination reactions give alkenes, like dehydration of…

Q: Identify A–E in the following reaction sequence.

A: Given,

Q: `NH2 HO. from b.

A:

Q: Br C=N

A: The given molecule synthesized in five step with different type of reagent which is shown in below-

Q: OH H3O* H20 он or он „CH3 H20 CH3 он

A: The mechanism for the following reaction is-

Q: NH3 =) - ف- منذ

A: Condensation Michael addition Reduction Hydrolysis Decarboxylation

Q: Ph Ph

A: Gilman reagent adds selectively to alpha-beta-unsaturated double bond.

Q: OH OH R. MgBr .R' 1. R' 'R' R. `R' OH 1. OsO4 2. H2O2, H2O ОН OH E A HCI H2O ОН

A: The given reaction is represented as follows:

Q: H 100 Br H ** CH3 NH₂

A: Given that, a synthesis scheme is shown below We have to carry out the above synthesis in two…

Q: H2SO4 H2O HO. H + ОН <

A:

Q: Diethyl malonate (CH3CH₂O₂C-CH₂-CO₂CH₂CH3) is treated with NaOEt followed by Br-CH₂CH₂CH₂CH3. The…

A: To identify the product we have to know the mechanism in details as follows

Q: Propose a multi-step synthesis pathway that utilize the indicated substrates to synthesize the…

A: sequence:- free radical bromination nucleophilic substitution

Q: 2.

A:

Q: MeO₂C CO₂Me 1. Reagents 2. Reaction Conditions 3. Mechanism CH3 O OH

A:

Q: 8) Consider the below desired transformation. Develop a retrosynthesis and forward synthesis that…

A: We have to convert methyl butyrate to 2-methylpent-2-ene

Q: 1. NaOH, heat 2. Neutralizing work-up O Select to Draw Br2 Br O Select to Edit H H

A: In the given reaction a carbonyl compound is treated with base followed by an acidic workup.…

Q: propose a synthesis

A: There are many mechanisms in organic chemistry such as nucleophilic substitution, nucleophilic…

Q: Perform the following retrosynthesis. (Provide the reactants and reagents required to convert the…

A:

Q: CH3 + a13- 29°C

A: The key step in this transformation is the formation of a stabilized anion by using pyridine and…

Q: Propose an efficient synthesis for the following transformation: 3-5- A The transformation above can…

A: Organic reactions are those in which organic reactant react to form organic products. In the given…

Q: Propose an efficient synthesis the following transformation: -C+ (C) The transformation above can be…

A: A cyclic ketal is formed when a ketone reacts with a diol. The ketal-forming reaction is catalyzed…

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.