Rank the following compounds in decreasing order of their reactivity toward the SN2 reaction with sodium ethoxide (Na+ -OCH2CH3) in ethanol.methyl chloride                tert-butyl iodide                     neopentyl bromide isopropyl bromide            methyl iodide                         ethyl chloride

Q: (stereochemistry)

A: We have to draw the structure of syn and anti addition of Br2

Q: CH3 H3C

A: Applying concept of nucleophilic addition reaction on carbonyl compounds.

Q: Give the SN2 product(s) for the reaction of (R)-2-bromopentane with an excess of sodium methoxide.…

A: Here we have to mention SN2 products for the reaction of (R)- 2-bromopentane with excess sodium…

Q: OH Specify a synthetic scheme that would produce the compound shown above in the fewest steps…

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Q: As shown below, pyridine -oxide G can undergo electrophilic aromatic substitution with electrophile…

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Q: Indicate, by letter(s), the position(s) on the ring at which substitution occurs when the aromatic…

A: F and OCH3 are weakly and moderately deactivating groups  to the ring (means that m-directive in…

Q: Rank the following compounds in order of increasing reactivity during electrophilic substitution…

A: Electophilic aromatic substitution reactions are the reaction in which a hydrogen atom has been…

Q: Write a mechanism that accounts for the formation of ethyl isopropyl ether as one of the products in…

A: When an alkene reacts with acid like HX then first it get protonated then X- attack to carbocation…

Q: By using "arrow-pushing diagram", draw the mechanism for each of the following reactions and predict…

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Q: Indicate, by letter(s), the position(s) on the ring at which substitution occurs when the aromatic…

A: Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Rank the compounds in each group in order of decreasing reactivity in electrophilic aromatic…

A: Electrophilic aromatic substitution reactions are the characteristic feature of benzene and other…

Q: Give the relative rates of reaction of the four carboxylic acid derivatives below with methylamine…

A: Thank you.

Q: Bringing together your knowledge of the reaction chemistry of substituted benzenes, suggest a…

A: Convertion of A to B can be done in two steps. They are,

Q: the  compound  can be synthesized by an SN2 reaction. Suggest a combination of haloalkane and…

A: Given:

Q: Given that the pKa of carbonic acid (H2CO3) is 6.4, is sodium bicarbonate strong enough of a base to…

A: Sodium bicarbonate, NaHCO3(aq) is a conjugate base of carbonic acid, H2CO3(aq).  For carbonic acid,…

Q: Br NH2 Br- COOH (a) NO2 (b) (с)

A: Answer:-This question is answered by using the simple concept of preparation of various oragnic…

Q: NO2 HBF4 Br, FeBra H2, Ni NANO2, H0*

A: We have to predict the major product from the given reagents.

Q: Aniline reacts with bromine in the absence of a Lewis acid to give monosubstitution products. Draw a…

A: The aniline is a strong activating group even stronger than phenols, ethers, halogens, etc. This is…

Q: arrange the following alkyl bromides in order of decreasing reactivity in an SN1 reaction:…

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Q: Triethyloxonium tetrafluoroborate, (CH3CH2)3O+ BF4 −, is a solid with melting point 91–92 °C. Show…

A: For the chemical reaction between triethyl oxonium tetrafluoroborate and Nuc:-, the chemical…

Q: For the reaction shown, select all suitable reagents: OH DMP CH₂Cl2 Na₂Cr₂O7, H₂SO4 H₂O PCC, CH₂Cl₂…

A: Among the given reagents:Strong oxidizing agentsWeak oxidizing agentNa2Cr2O7, H2SO4, H2ODMP,…

Q: Which of the following is the best method to carry out the following transformation? - OH (a) H₂SO4,…

A: We will draw all the product of each reaction.

Q: он OH OH он OCH3 CI CH3 10.0 10.2 9.2 7.7

A: Give an explanation, why the acidity of these phenolic derivatives give these pKa value?

Q: Give the major organic product(s) for each step of the following sequence of reactions. Write NR if…

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Q: Which of the following is a substrate product when benzene is first treated with HNO3 and H2SO4, and…

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Q: 4. Complete the outlined reaction sequence by drawing structures for the major products expected.…

A: A species with a larger size can easily accommodate negative charge. In other words, in a large size…

Q: Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of…

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Q: Suggest a reasonable series of reagents and reactions conditions to prepare cis-2-methylcyclohexly…

A: In the reactant, both Me and OH groups are present at axial position. At first OH group is oxidized…

Q: Give a full arrow-pushing mechanism for the following acid-catalyzed reaction: HC1 H₂N.

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

Q: Provide the structure of the reactants necessary to prepare the following compound using the Wittig…

A: The structure of the reactant needed to prepare the given product using wittig reaction = ?

Q: None

A: Step 1: The reaction involves a Friedel-Crafts acylation, which is a type of electrophilic aromatic…

Q: Describe the mechanism by which benzene is converted to bromobenzene (C6H5Br) on treatment with a…

A: Benzene reacts with halogen in the presence of Lewis acid to form aryl halides through electrophilic…