Step 2: Complete the resonance structure of the keto form, then add curved arrows.   Step 3: Complete the resonance structure of the enolate form. Omit curved arrows

Q: Propose a mechanism for the reaction. Fill in the missing curved arrows in each step.

A: The given reaction is of dehydration of alcohol to alkene

Q: Draw (HC(CH3)2)2

A: During drawing structure, we have to keep in mind that carbon forms four bond.

Q: draw the major product. HO SO3 H2SO4

A: Step 1: Step 2: Step 3: Step 4:

Q: Draw the reactant of the following reaction. 모 ? H heat

A:

Q: Draw the product of attached reaction.

A: The substrate in the given reaction is epoxide. The given reaction proceeds through epoxide ring…

Q: Draw a reaction energy diagram that corresponds to the following reaction. conc. H,SO4 -HO-

A:

Q: Draw a stepwise, detailed mechanism for attached reaction.

A: A detailed mechanism for the given reaction can be drawn as,

Q: S. H* v the protecting group reactant. ect Draw Rings More

A: When we used the retrosynthsis means reverse to synthesis then we can easily identify the reactant…

Q: Add curved arrows to the reactants in this reaction. A double-barbed curved arrow is used to…

A: Introduction: The compound which donates H+ ions and the compound that accept H+ ions is called acid…

Q: Curved arrows are used to illustrate the flow of electrons. Follow the arrows and draw the…

A:

Q: Draw the primary organic products in the box. heat +enatiomer

A:

Q: H2 H,0, H* CH3 H3C. H2C 1. CH,

A: This compound is a ketal having two different alcoholic arms. So, after hydrolysis it produces two…

Q: Draw the mechanism using curved arrows for the given reaction. Try one last time + ☐ :Ö-H +…

A:

Q: Draw the product of attached reaction.

A: The mechanism is as shown below:

Q: What is the product of this reaction? F d Br FeBr3

A: To solve this problem we have to complete the given reaction .

Q: Complete the resonance structure of the keto form and add curved arrows

A: Applying concept of resonating structure of keto to enol form.

Q: H3CO. 1. NaOCH3 2. H20 OCH3

A: Any molecule or ion which are electron rich species are called nucleophile for example -NH2,-OH and…

Q: 4. Synthesize the following compound starting with the halide shown. All carbons must come from…

A: Guidelines detail

Q: Circle the most reactive molecule with water and put an X through the least reactive. CI

A: The molecules are acid derivatives:

Q: Draw a stepwise, detailed mechanism for the following reaction. Use curved arrows to show the…

A: Br acts as leaving group and CH3CH2OH as nucleophile, which results into formation of nucleophilic…

Q: " Complete this mechanism for an acid-base reaction by adding curved arrows. ← H :0: H ☐ H…

A: This question belongs to enolate chemistry. Formation of enolate ion will take place after…

Q: он Br

A:

Q: Draw a stepwise mechanism using arrows to show electron movement and drawing each intermediate…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: Draw the products in attached reaction?

A: A chemical reaction mechanism represents the way to form and break the chemical bonds between…

Q: draw the step one product and draw curved arrows to show the nucleophilic addition step.

A: To provide the arrow mechanism for the first step of the Fischer esterification reaction and the…

Q: the major pr byproducts.

A: A question based on the reactions of alkenes with 1) Hg(OAc)2, H2O 2) NaBH4, NaOH. THis reaction is…

Q: Draw the products of attached reaction by following the curved arrows.

A: Given:

Q: ОН K2Cr2O7 H₂SO4

A:

Q: H₁ H KOH EtOH heat

A: The question is based on organic reactions.     we need to identify the product formed and explain…

Q: Draw the expected product of the given reaction. H HBr H Strategy: Identify the type of reaction…

A: Addition of HBr to unsymmetrical alkenes (3,3-dimethylbut-1-ene) :When the alkene (…

Q: 5F15NH2 H2O

A: Aniline is simplest organic compound  and it is simplest aromatic amine and it consists of  phenyl…

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.