Solvent of reaction is methylene chloride. Part a) Draw arrow-pushing mechanim. Show ALL resonance structures in it also

Q: Show the curved arrow formalism in order to arrive in the major final product

A: This reaction proceeds via an electrophilic addition mechanism. This reaction proceeds in a…

Q: 3- Prove by discussing the aromaticity of the molecules given below. Gint

A: Aromaticity is a property of cyclic, planar structures with a ring of resonance bonds that gives…

Q: Using the information below explain why CN- is a stronger Bronsted base even though in the reaction…

A: Bronsted base is the species that accept proton.

Q: draw resonance structures and label major contributor

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Q: Nucleophilic attack may appear to occur in two steps as shown below. The alcohol is the nucleophile…

A: The carbon atom double bonded to oxygen atom and single bonded to two alkyl groups is called…

Q: A proton transfer reaction can occur when an aldehyde is placed in strong base, such as an alkoxide…

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Q: c) Circle the most electrophilic carbon in the structure below and explain your choice.

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Q: Terminal alkyne is considered a more acidic compound because it has a lower s character. True or…

A: In this question, we will discuss about this Statement is true or false.  You can see details…

Q: a) Which of the following compounds is (are) capable of H-bonding to itself? Circle all that apply.…

A: Given compounds are: In the above given compounds, A is a ketone, B is an alkene, C is alcohol, D…

Q: H "F

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Q: can someone help me determine the following reaction that would result with the following reactants?…

A: In a Grignard reagent, an alkyl group is attached with electropositive metal, magnesium, which acts…

Q: с.

A: Resonance structures are madeup via flow of electrons.

Q: :0:

A: Nucleophilic substitution reactions: these are the type of reactions in which nucleophile reacts…

Q: 2) For two of the following pairs of compounds, identify the most basic atom in each compound, and…

A: Here we have to find the most basic atom and the most basic compound from the given pair of…

Q: Write any specific net reaction of your choice, which represents some type of reaction mechanism…

A: Hello. Since your question has multiple parts, we will solve the first question for you. If you want…

Q: Of the above compounds, which is least basic? Of the above compounds, which is least nucleophilic?…

A: Nucleophilicity is the tendency of the atom to donate electrons. Negative charge is more stable on…

Q: Write any specific net reaction of your choice, which represents some type of reaction mechanism…

A: Hello. Since the question contains more than three sub-parts, the first three sub-parts shall be…

Q: In the following species, circle the most acidic hydrogen:

A: Acidity is defined as the tendency to release H+ in the solution. When H+ is removed then a negative…

Q: What is the most acidic hydrogen on the following molecule and why?

A: A strong acid is an acid that dissociates to make protons available for reaction. Acid mainly…

Q: So, in this lewis acid-base reaction, do we need to draw lone pairs or not? Why or why not? Thank…

A: In the given lewis acid base reaction :  Is it necessary to represents the lone pair of electrons ?

Q: (c) Nitrobenzene will undergo electrophilic aromatic substitution at meta position, but not at the…

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Q: Molecule A is more acidic compare to the molecule B? Why explain

A: In this question, we will discussed about why molecule-A is more acidic than molecule-B.  molecule…

Q: What would be an appropriate term to describe molecules B and C? in A В Me `Me Me resonance…

A: Molecule A is conjugated. B and C are skip diene

Q: how do we know which one is carbon 1 ，which one is carbon2？Did I draw the compound correctly？Step by…

A: According to IUPAC namenclature whenever the more than one substituents are attached the namng order…

Q: Do your protons correspond to aldehyde or ketone functionality? Explain why or why not. Are any…

A: To determine which group is attached to the compound A or what functional groups present in the…

Q: Now point out (Circle) the MAJOR CONTRIBUTOR(S) in you need consider all the resonances including…

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Q: Detailed acid and base reaction and use arrows and give conjugate acid and tase along with the arrow…

A: Bronsted- Lowry acid-base theory :  Bronsted acid : Proton (H+ )  donar is called Bronsted acid…

Q: Draw curved arrows to show how one resonance contributor leads to the next one.

A: a) Please find below the resonance contributors.

Q: of the radicals?

A: 1.Resonance  structure  is represented by the lewis structures and actual structure  is hybrid of…

Q: Explain (using resonance forms and words ) why compound 1 undergoes hydrolysis faster than compound…

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Q: In the picture, Each of the following compounds has more than one kind of (a-H's). First draw all…

A: see the picture uploaded in the solution.  the most acidic proton is circled. if more than one…

Q: Add the hydrogens to the following structure and circle its most acidic hydrogen(s).

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Q: For molecule showed on the rightdraw the structure of 3 different conjugated basesbased on 3…

A: Resonating structures are lewis dot structures that are produced from the delocalization of electron…

Q: And Allyl / Phenyl compound are most reactive towards SN2 because of resonance stabilization. then…

A: SN^2 reaction is a single step process. SN^1 reaction is a two step process. SN^1 reaction involves…

Q: Why does Hammett Equation only apply to meta and para substituted rings and not others? Explain

A: The Hammett equation in organic chemistry describes a linear free energy relationship relating…

Q: from and alcohol of two carbon or less Cl

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Q: Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Long and detailed explanations…

A: When you mixed both in equal about then compound C not rotate plane polarized night because this…

Q: Part 3 out of 4 Select the compound that results from the reaction with following resonance…

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Q: Weak base can react with strong acid to form a salt. If pyridine reacts with a strong acid to form…

A: Aromatic compounds are conjugated, planner and have ( 4n + 2) delocalizable  electrons.

Q: last three compounds. Compound à Aromatic/Anti-aromatic/ Non-aromatic fptanar :O: NH

A: Since you have posted a question with multiple sub-parts, we will solve the first three subparts for…

Q: What is the correct order of the words in the blanks in the following sentences? If there are…

A: The different properties of the substituents on the benzene ring depends upon the type of group…

Q: Redraw the following molecule and circle the two sites where nucleophilic addition is possible for…

A: The questions are based on the concept of organic mechanism. we have to identify the site where…

Q: Please circle the most acidic hydrogen(s) in the molecule below

A: Alcohol are more acidic then alkynes .

Q: A. Draw all significant resonance structures of each compound below, using appropriate arrows, and…

A: Here we have to draw the resonance structure of the given compound and then we have to indicate the…

Q: Draw all the resonance structures of A and circle the major contributor.

A: Resonance structure:If the Lewis structure of a molecule or ion cannot explain by a single structure…

Q: Question Consider molecules A–D. Does the arrow pushing in each structure lead to an acceptable…

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Q: Consider the below molecule and its hydrogen atoms labeled a through e. Rank the named hydrogen…

A: acidity -  increase order -  Hd<Hc<He<Ha<Hb

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.