The reaction shown involves an acid chloride, draw the organic product and select the inorganic species present at the end of the reaction. The structure of the acid chloride is drawn for you as a starting point, so you need to modify it to draw the reaction product. May you also draw the mechanism please to show how you got the organic product with the inorganic.

Q: NaOH CH3 CH3 2

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

A: The Bronsted-Lowry acid-base theory states that the acid is a substance that gives H+ ions and the…

Q: H3C OMe Phys-C(CH3)2 DMSO

A: The reaction is known as Johnson–Corey–Chaykovsky reaction. This reaction is used for the synthesis…

Q: Draw the reaction mechanism showing bonds that are broken/formed

A: The reaction is hydrolysis of amide and the mechanism

Q: НО. H3O+

A: Product of following reaction can be made by applying appropriate reaction mechanism.

Q: CHO + CH 3 CH 2 NO ₂ 113

A: The reaction which is between nitroalkane and aldehyde or ketone in presence of base C-C bond…

Q: Confused on how to continue with this mechanism reaction

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Q: Simple Reactions) Draw the products for each reactions that are shown.

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Q: For the reaction can someone please synthesize the given products from the given reactants. Multiple…

A: The explanation of the organic reaction is given below

Q: LIAIH4 H20

A: Lithium aluminium hydride is a very good reducing agent used in the reduction of aldehydes, ketones,…

Q: OMe OHC, KOH/ N OMe ÓMe OMe OMe ÓMe

A: Nucleophilic addition reaction: Addition reaction in which an nucleophile is added to electrophilic…

Q: он Br

A:

Q: 1/2 Fe203 (s) + 3/2 CO (g) ® Fe(s) + 3/2 CO2 (g) DH = -11.5 kJ 3 Fe2O3 (s) + CO (g) ® 2 Fe3O4 (s) +…

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Q: Consider the reaction between 2-methyl-2-butanol and HBr, shown below. HO HBr Br

A: Given that, the reaction is:

Q: H2SO4 OH heat

A: Alcohols react with sulfuric acid in presence of heat and undergo dehydration reaction producing…

Q: 13 of 36 > Consider the pair of reactions. Draw the organic products, then predict the type of…

A: We know in presence of strong nucleophile secondary halide can undergo SN2 reaction in which rate…

Q: MCPBA to Ph alkene

A: mCPBA is the short form of m-chloroperbenzoic acid. It reacts in a concerted way, that is,…

Q: Consider the reaction below. a) Predict the reaction mechanism that is likely to operate between…

A: The given reaction is an example SN1 reaction stands for substitution nucleophilic unimolecular. The…

Q: H2C H2C CH2 Н—с-он н—с-о, 2 H2C B(OH)4 H2C CH2 + + 4 H Н—с—он H FC-o о—с—н H2C H2C CH2 PVA temporary…

A: Applying concept of nucleophilic substitution reaction on boron center.

Q: CeHgLi

A: Introduction :  We have to tell the product for this reaction .

Q: NH2 Но CF3 CF3 +

A: Here we have to determine the correct starting material that can reacts to produce an amide. Here…

Q: Heat Benzaldehyde + KCN + EtOH

A: Concept introduction: Benzoin condensation: It is the coupling reaction that is occur between the…

Q: Show the mechanism for the given reaction conducted at -5 "C in CCI,. cyclohexene + bromine –…

A: Bromination of alkene is an addition reaction in which the bromine atoms will add across the double…

Q: 1.NaH/MDSO/CH3I 2.HNO3/H,SO4 3.Fe/HCI CH3 H3C 'N' NH 4.1.HCCOH/Heat 2.HNO/H2SO4 'N' N.…

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Q: Draw the products of each reaction, and label the nucleophile and electrophile. (see the attachment)

A: SOLUTION: Step 1: In the reaction of diethyl ether and boron tribromide, diethyl ether is a…

Q: CH2- HI

A:

Q: After drawing a mechanism for this reaction determine which intermediate cannot be formed. A H…

A: A question based on reaction intermediate. Five options are given, the most inappropriate…

Q: R-O-O-R

A: This is Free radical decarbonylation. 1st product is without radical rearrangement via less stable…

Q: H. CI

A: The given reaction is a simple SN1 reaction of 2 methyl propane with HCl to form 2 chloropropane.…

Q: H CH3 A cyclopentyl methyl ketone Show the mechanism of a crossed aldol reaction starting with…

A: Given: two compounds. To show: crossed aldol reaction starting with cyclopentyl methyl ketone and…

Q: HO cat. H+ 1 equiv. EtOH - H₂O

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Q: Et20 :ộ: MgBị: Mg.

A: Since there is partial +ve charge on C in Hence it will be attacked by the -vely charge species as…

Q: H3C, CH3 H3C N. HN. HO, N. N. ČH3 ČH3

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Q: NOZ NOZ Nat o-Cts (Sodium metho xide) CI OCHS CH3 NO2 NO

A: Given reactions are : 1). Aromatic nucleophilic substitution reaction and  2). Aromatic…

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.