Сно NaBH4 H2CrO4 А В base CHO OH PHCHO ILot

Q: 1)DCC 2) OH IZ ZI

A: Amides are carboxylic acid derivatives where the -OH group of the acid has been replaced by -NH2,…

Q: The mechanism for the synthesis of biodiesel is not a nucleophilic aryl substitu OGMU 2020 749692 O…

A: The question is asking whether the process of synthesizing biodiesel involves a nucleophilic aryl…

Q: II H3CH2CH=CHCH2CH=CH(CH2)4C-OH NaOH

A: In this question we want to determine the Product.  How we can determine you will see below details…

Q: CH3

A: In this question, we want to Synthesized final product from the starting material by using Reagents.…

Q: what are the major products off these reactions.

A:

Q: Draw the product(s) of the following acid-base reaction. OH O O + HOSOH

A: The objective of the question is to determine the product(s) of the given acid-base reaction. In…

Q: Synthesize the o-form of amino benzoic acid from benzene.

A: Synthesis  of  o-form of amino benzoic acid from benzene is given below

Q: II) Draw the products for the following reactions H2 Br2 HBr H20

A: The reactions given are,

Q: OH H+

A:

Q: H -СН+ 2СHCH-ОН

A:

Q: Draw the reaction mechanism of the following reaction. In the textbox below, name the reactant and…

A: Given reaction is hydrochlorination reaction. Addition takes place according to Markonikov's rule.

Q: Draw the structures of the following peroxides: m-chloroperbenzoic acid di-t-butyl peroxide…

A:

Q: Provide the product and mechanism for the reaction: ОН CrO3, H,SO, H,0

A: This reaction is an example of Jone oxidation. Mechanism of Reaction:

Q: Draw the product(s) of the following reaction: Ph3P=CH₂

A: Carbonyl compoundsl reacts with phosphorus ylides to form alkene.alpha, beta-unsaturated Carbonyl…

Q: Draw the carbon containing products of the following reaction: Reactant = 2-bromo-2-methyloctane…

A:

Q: CI CN NaCN H3C CH3 H3C CH3

A:

Q: Consider the following reaction. Predict all products and determine which one is the major product.…

A: Substitution nucleophilic unimolecular reaction is given as SN1 reaction. SN1 reaction goes through…

Q: How do you synthesize a cyclohexane-1,2,3-triol from a cyclohexane

A:

Q: -ССH3 + CH3OН H+

A: Ketone and alcohol react with each other in presence of H+ to obtain ketal type of compounds. Here…

Q: What is the product of the following reaction?

A:

Q: 2) Draw all products formed in the following SN1 reaction. Br CH;CH2OH

A:

Q: draw the carbon containing products of the following reaction: Reactant = 2-bromo-4-methyloctane…

A: We have been provided with the reactant and reagent and we have to find out product:

Q: Provide the major products for the following reactions?

A: The mechanism of the given reactions are

Q: Br CH3OH

A: Reaction of Given compound with methanol give products by both SN1 and E1 reactions.

Q: 2. Draw the mechanism of the following reaction. Show how all of the following products form.…

A:

Q: Draw the structures of all the possible products that can be obtained from the dehydration of…

A: Alcohol is an organic compound that has OH functional groups.They are reactive due to the presence…

Q: Draw the final product(s) of the following hydroboration-oxidation reaction of an alkyne: 1)…

A: Disiamylborane is used for hydroboration–oxidation reactions of terminal alkynes. In the…

Q: 1) CH;OʻNa* Br

A:

Q: H2O

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.