Propose a synthetic route to the desired prodet from te given startiry material. Include all reuges and sythetic interwediutes. へ.

Q: Plan a synthesis of congored?

A: Congo red is an organic compound and is a type of an azo dye, it is a water soluble compound and…

Q: Devise a synthesis of HC≡CCH2CH2CH3 from HC≡CH and any other organicor inorganic reagents ?

A: The synthesis reaction will have below steps. 1) reaction of HC≡CH with 1 mole of NaNH2 to form…

Q: propose a plausible synthesis

A:

Q: Chemistry Help woth this three retrosynthesis. thank you Provide a retrosynthesis and a forward…

A: TM 1 : Epoxide opened with 1-napthol. TM 2 : see below. TM 3 : Ethyl benzoate is subjected to Fridel…

Q: From the given structures which is (a) an acid halide? (b) a secondary amide (c) an aldehyde…

A:

Q: tow is benzophenone suited for nueleophilie aromaic abstitution Which positions and the be…

A:

Q: Draw the Configuration of the D-Family of Aldoses in a short bond paper (fit in 1 page only) Label…

A:

Q: OH Br NBS NaOH Acetone/H,O limonene bromohydrine limonene oxide

A:

Q: nthesis, show two different synthesis strategies. In the first synthesis strategy, include e…

A: The questions based on organic reactions. We have to convert the reactant into product by a series…

Q: F;C. HCI ZI

A: IMPORTANT POINTS: In this type of question where precursor is asked ,here hypothetical hit and…

Q: Propose a mechanism for the following reaction:

A:

Q: Draw the product formed from the ring-closing metathesis of eachcompound. Then, devise a synthesis…

A: 1- First we will see tha Products for each by using ring closing metathesis.

Q: Show how the anisole can be synthesized from benzene:

A: Anisole is a methoxy group attached to the benzene ring.

Q: Ph Ph МСРВА Но HO.

A:

Q: The reaction below is homogenic homolysis heterolysis heterogenic

A:

Q: (b) Provide the retrosynthesis along with forward reaction for the the following compounds as…

A: Retrosynthesis is the imaginary breaking of bonds of the molecule in such away that the molecule is…

Q: Complete Mechanism for the deuteration of acetone on treatment with D3O+

A: Deuteration reaction :  Due to Acidic nature of the hydrogen at alpha position in ketone these…

Q: CHS H.

A:

Q: Draw the major product(s) of nitration of benzoic acid.

A:

Q: What acetylide anion and epoxide are needed to synthesize attached compound?

A: Applying retrosynthesis approach, we will get our desired acetylide anion and epoxide.

Q: Propose an efficient synthesis for the following transfor X (a) OF

A:

Q: How would you synthesize olestra from sucrose?

A: The synthesis of olestra is shown as,

Q: to

A: This synthesis involves Michael addition, Aldol condensation, dehydration, hydrolysis and…

Q: What epoxide and organometallic reagent are needed to synthesize attachedalcohol?

A:

Q: Rank the species below in order of increasing nucleophilicity in protic solvent.

A: Nucleophile are species which have excess of electron density either have filled orbital or lone…

Q: Propose a synthetic method for the following compound:

A: The given compound can be prepared by using benzene which shows electrophilic substitution of…

Q: propose the retrosynthesis of the following compound

A: The retrosynthesis of the given compound is-

Q: Explai all steps to Determine the Directing Effects of a Particular Substituent ?

A: The characteristic reaction shown by benzene and other associated compounds is electrophilic…

Q: Synthesize attached product from the given starting materials using an organocuprate coupling…

A: Product from the given starting materials using an organocuprate coupling reaction has to be given.

Q: Devise a synthesis of attached biologically active compound from benzene

A: The mechanism of formation of acetaminophen from benzene will be shown where firstly, the nitration…

Q: From the given starting material provide a reasonable synthetic route to the following plecule. O,N.

A: Here we have to prepare the given compound from the starting material 2-methylbuta-1,3-diene in…

Q: 4. Provide a retrosynthesis only. Ph Ph Ph Ph

A: Retrosynthesis of the following compounds is given below.

Q: Provide a retrosynthetic analysis and forward synthesis for the compound shown below. and any other…

A:

Q: Show the complete mechanism for the formation of a hemiactetal, when 3-methyl-2-butanone eacts with…

A: Ketone with 1 equivalent of alcohol in acidic medium forms hemiacetal.

Q: here would you cut during retrosynthesis for the following molecule 4 1l ansuuers

A: Given target molecule is beta hydroxy ketone , which is product of aldol condensation reaction.

Q: How To Synthesize a Compound Using the Robinson Annulation ?

A: Given:  Synthesize a Compound Using the Robinson Annulation

Q: a La =C

A:

Q: tage yield ðf the product.

A: limiting reactant  It is a reagent that is completely used in a chemical reaction and when they…

Q: (b) Provide forward reaction) compounds provided : (i) (ii) NC suitable retrosynthesis for the CN as…

A:

Q: 4. Provide a retrosynthesis only.

A: Retrosynthesis : at first three ethers are cleaved to give corresponding alcohols. Then functional…

Q: how an alkene be coverted into carbonyl compound in one step?

A: Ozonolysis: The unsaturated bonds (double, triple or azo compounds) are cleaved with reductive…

Q: the nucliophile and of ing Heaction. Give a Meactions using cunved AMHOWS electmophile in each step…

A: Nucleophile is an electron rich species and electrophile is an electron deficient species.

Q: Propose a forward synthesis for one of the two sequences below using whatever reagents necessary. Do…

A:

Q: 17. Provide a curved arrow mechanism for the following transformation. Br NaN, DMSO

A: As shown in the reaction, the rection follows SN2 pathway because the product is inversion in…

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.