Please draw the mechanism for the following reaction. The first step in the reaction mechanism is the formation of a carbocation intermediate (shown), followed by a carbocation rearrangement.  Which bond moves in the carbocation rearrangement?  Which compound shown below has that appropriate bond in pink?

Q: Which of the following compounds is most reactive under E2 conditions? Br Br Br (A) (B) (C) (D)…

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Q: Draw the molecules on the canvas by choosing buttons from the Tools (for bonds and charges), Atoms,…

A: LiAlH4 is a strong reducing agent which reduces carbonyl compounds (ketones, aldehydes, esters,…

Q: Write the mechanism of the following bromination reaction and explain the regioselectivity of the…

A: This is due to difference between the rate with which chlorination and bromination occurs by free…

Q: CH3 NaOH

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

Q: Question 3 Draw the mechanism and final product for the following reaction. IR (cm-1): 3307, 3295,…

A: There is error in last step only. As N has one H left so when H2O will leave and N shares its lone…

Q: Но OH FeCl3 + H3C `CH3

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Q: Stereochemistry for the following reaction Br2, H20

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Q: Review the SN1 reaction below: CI OCH 3 CH3OH + + CH3OH2 + Now consider the energy diagram for the…

A: In the study of organic chemistry, the SN1 reaction mechanism is a fundamental concept, particularly…

Q: Alkyl diazonium salts (shown below) are considered "super" leaving groups; a consequence of this is…

A: Alkyl diazonium salts are the excellent leaving group because R- N2+ because nitrogen is an…

Q: In the reaction shown below, which of the following is the nucleophile? OCH₂CH3 CH3CH₂CHCH₂ + 2…

A: A nucleophile is a reactant which gives an electron pair to form a covalent bond. A nucleophile is…

Q: Rank the following in order of increasing reaction rate with Br2 (slowest to fastest)

A: The objective of the question is to rank the given alkenes in order of increasing reaction rate with…

Q: Complete the following reactions by providing the proper substitution AND the proper elimination…

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Q: CN- I"H Br

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Q: The molecule, 2-bromo-1,3-diethyl-1,4-dimethylcyclohexane undergoes an SN1/E1 reaction in the…

A: i. In the first step the leaving group Br departs to give carbocation.  ii. Due to migration of most…

Q: dissociation NaBr Select to Draw Carbocation Intermediate Carbocation Rearrangem ent Select to Draw…

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Q: Draw the major product of this reaction. Ignore inorganic byproducts. NO2 1. LIAIH4 2. H3O*

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Q: In Part 1. choose the most "electron-rich" atom in the reaction below. In Part 2, identify the…

A: The given reaction is a nucleophilic substitution reaction. In this reaction, sodium ethoxide acts…

Q: OH H2SO4 Нeat

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Q: .CH3 NH3 H Br +

A: Organic reactions are those in which organic reactant react to form organic products.

Q: Drawing the Products of an SN1 Reaction Label the nucleophile and leaving group, and draw the…

A: the nucleophile and leaving group

Q: When ethylbenzene reacts with bromine in a free radical halogenation, a small amount of product that…

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Q: 3. Both El and E2 reactions are possible with 3° alkyl halides. Which elimination mechanism would be…

A: A question based on reaction mechanisms. A reactant and two possible elimination products are given…

Q: Br Q 5) Consider the two E2 reactions above. Br NaOH DMF heat NaOH DMF heat a. What are the major…

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Q: When an unsymmetrical Alkenes such as propane is treated with N-bromosuccinimide in aqueous dimethyl…

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Q: Identify the elementary step

A: Given reaction:

Q: Br2, FeBr3

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Q: How many acid-base steps occur in this mechanism? :OH :OH ₂ H CI: -H₂O (C5H₁2O) (C5H130+) (CgH*)…

A: Acid : Proton donar. HCl is acid because it will provide protons. Base : Proton acceptor. Here…

Q: 11. Determine whether each reaction occurs by an SN2, SN1, E1, and/or E2 reaction. Provide a…

A: Conditions for the SN1 , SN2 , E1 and E2 reactions;  Good nucleophile, 1° and 2° alkyl halide and…

Q: ng is most reactive under E2 conditions? Br Br Br Br (A) (B) (C) (D) Compound B Compound C Compound…

A: Applying condition of E2 elimination reaction.

Q: HCI HO ZnCl2

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Q: If H1 is eliminated from the carbocation shown here in an electrophile elimination step, then three…

A: In E1 mechanism, a carbocation is formed first and then a double bond by the abstraction of proton.…

Q: The resonance stabilized carbocation formed in step one has two electrophilic centers draw. The…

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Q: Write the mechanism of the following bromination reaction and explain the regioselectivity of the…

A: Regioselectivity => When one product is formed in major amount over another product in a…

Q: Fill in the table below indicating what is important in each category for an SN1 reaction and an SN2…

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Q: alcohol. A carbocation intermediate is central to which of these reaction types? (circle) E1 E2…

A: In bimolecular reactions the attack of nucleophiles (in case of SN2) or base (in case of E2) and…

Q: 4. The cis isomer of 4-tert-butyl-1-bromocyclohexane undergoes E2 eliminations about 1,000 times…

A: These are the examples of E2 reaction

Q: Will each of the following reactions follow an El or E2 mechanism? CI HO Он

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Q: Which of the following compounds reacts faster in an elimination reaction with KOH? Also provide the…

A: Alkyl halided given E2 elimination reaction with KOH. In the E2 elimination reaction, the removal of…

Q: Select the arrow drawing that best describes this step of an E1 reaction. H I-0: І H3C I нн i 1-0:…

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Aromatic Compounds

Aromatic organic compound or aromatic system is an important class of hydrocarbons under the branch of organic chemistry. Aromatic compounds are also called arenas. The definition of aromatic organic compounds can be stated as a class of organic compounds with a planar cyclic ring of atoms bonded through alternated single and double bonds. Due to these alternating bonds, a peculiar feature termed as ‘resonance’, that is, delocalization of pi electrons or the electrons is shared within the atoms of the ring which are present in the aromatic compounds. The word ‘aromatic’ includes a Greek word ‘aroma’ which means smell, indicating that they were named as such due to the sweet odor they produce. Many well-known flavors such as vanilla, cinnamon, and few scents from flowers are extracted from aromatic compounds. Benzene with chemical formula C6H6 is a very common aromatic compound that contains six atoms of carbon held in the cyclic ring of alternate double bonds. It is also to be noted that not all aromatic compounds contain benzene ring. This can be explained by Huckel’s rule.