Complete the synthesis of the following product from benzene and the given reagents. COOH CH3C1 KMnO 4 HNO3 [A] [B] AIC13 H₂SO4 I draw structure ... [A] edit structure ... [B] NO₂

Q: Draw the organic products of the reaction shown. Draw hydrogens on oxygen and nitrogen where…

A: We know that imines contains  C = N  bond These are readily reaction with acid and water conditions…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. HBr (1 equiv) Drawing

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Q: SOCl, heat

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Q: What is the major product of the following reaction? OH H™ A/

A: One mole Alcohols add reversibly to aldehydes  to form hemiacetals

Q: Show how you would make the target molecule from the provided starting structure. Show all…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: Draw and name the organic product of the given reaction. \(\ce{ {} + HNO3 ->[\large\ce{H2SO4}][]}\)…

A: Benzene and its derivatives undergo electrophilic aromatic substitution reactions when treated with…

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

A: Step 1: Step 2: Step 3: Step 4:

Q: Please answer a,c,d,f

A: Since the nucleophile will attack on the propyl iodide and replace the I. Hence the nucleophiles…

Q: Please rectant and product name and give ?mark

A: Solution-  Reactant and product and reagent name are given below by the above reaction-

Q: Esters have two unique sides.  When looking at an nmr spectrum the hydrogens alpha to the carbonyl…

A: Esters have two NMR active Hydrogens 1) Alpha to Carbonyl Carbon 2) Alpha to Oxygen atom of Ester…

Q: In the drawing area below, create an acetal with 1 ethoxy group, 1 methoxy group, and a total of 6…

A: Acetal is an organic compound which can be represented using the following general formula-Here, R,…

Q: `CI AICI3

A: In Friedel crafts alkylation, the first monoalkylated compound will again undergo an electrophilic…

Q: ÇH3 ÇH3 4 VIEW SOLUTION 17 OF 25 QUESTIONS COMPLETED

A: Hydrogen bond  is electrostatic force of attraction between a hydrogen (H) atom which is covalently…

Q: 10. For the Tollowing, uSE UND a) Write out 6 completely different reactions of 3-pentanone…

A: Here the key functionality is ketone and the carbon atom present in it is very much facile towards…

Q: nitrogen, where appropriate. (2 equiv.) CI Select Draw Templates More // с H N Cl Erase

A: It is based on the reactivity of acid chloride. Here we are required to predict the major  product…

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: Reaction B. Draw the product of reaction B. Select Draw Rings C H O Ć More Erase Q2 Q

A: Claisen condensation : Condensation of esters produces β keto esters in the presence of NaOEt and…

Q: ® which of the fillowing Erplain. aromatic, antiaromahe or nonaromMai are a) (9 f)

A: Condition for aromaticity are: 1. The molecule should be cyclic and planar. 2. The molecule should…

Q: You didn't answer D&E

A: An acid is a species which donates proton while a base is a species that accepts proton.    An acid…

Q: Draw the organic product you would expect to isolate from the nucleophilic substitution reaction…

A: Given reaction is an example of nucleophilic substitution reaction.The substitution reaction is a…

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: Please draw the missing products and PLEASE answer A through E. I think I got A and B but I really…

A: Both A and B parts you have done are correct. We will solve the rest three question.   C. The given…

Q: Step 1: Draw curved arrows. Select Draw Templates More. / |||||| C Br iz: N M + Na . Erase Step 2:…

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Q: NBS, ROOR

A: The reaction taking place is given as,

Q: ОН ОН

A: Note: The reaction is example for pinacol pinacalone rearrangement. Mechanism: Step 1: stable benzyl…

Q: Draw the ester electrophile that would be needed to make this product through a Claisen condensation…

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Q: Draw the product of the reaction shown below. Ignore inorganic byproducts. Zn(Hg) HCI

A: This is an reduction reaction.  Where ketone is reduced to direct alkyl group.

Q: Macmilla Determine the products in each acid-base neutralization reaction. NH NH₂ HCI HF Select…

A: An acid–base reaction is a type of chemical reaction that involves the exchange of one or more…

Q: What is the product? OA B. apl o O CI AICI3

A: Given,The reaction:

Q: 5. What important intermediate is made from the reaction of 2-hexanone with an acid in the presence…

A: A question based on reactions of ketone. A ketone reactant is given whose product of reaction with…

Q: Draw the major products of the elimination reaction below. If elimination would not occur at a…

A: The objective is to determine the product of the given reaction.

Q: Show how you would make the target molecule from the provided starting structure. Show all…

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

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: None

A: Alkyl chlorides undergo two main types of reactions: nucleophilic substitution and elimination…

Q: 2 CH3CH2NH2

A: An organic chemistry based problem, which is to be accomplished.

Q: دے you CH

A: Cyanobenzene, more commonly known as benzonitrile, is an organic compound with the chemical formula…

Q: Draw the monoalkylation product of an amine reacting with methyl iodide. Ignore any inorganic…

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Q: None

A: Step 1: The organic reactant: This is the cyclohexanone molecule (the six-membered ring with an…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Pl +O°H Select to Draw

A: This is a hydrolysis reaction being carried out in presence of acid to form alcohol. The formation…

Q: Add curved arrow(s) and the products to complete the second step of the E1 mechanism, where the…

A: In the E1 mechanism, where E1 is stand for unimolecular elimination. It is two steps mechanism.

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.