Rank the following organobromides in order of increasing rates of ionization to its carbocations and Explain the trend. Br -Br -Br CH3

Q: (i) (ii) NaOH (iii) SOCI₂ heat (iv) CH₂N₂ (2 eq.) (v) Heat, EtNH₂ C12H21 NO2

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Q: Considering only electron density, state whether the following reactions will occur: a. CH3CH2-Br…

A: Electron rich species are those which bear a lone pair of electrons, pi bonds or have negative…

Q: The 2-propenyl cation appears to be a primary carbocation, and yet it is considerably more stable…

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Q: Which of the attached compounds undergo Friedel–Crafts alkylation with CH3Cl and AlCl3? Draw the…

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: 33. Arrange each set of compounds in order of reactivity towards the E2 process. Br Br Br CI (a) (b)

A: Interpretation-  To arrange set of compounds in the order of reactivity towards E-2 process .…

Q: I I Least reactive Most reactive

A: SN1 reaction is substitution nucleophilic unimolecular reaction. Stability of reaction depend upon…

Q: Rank the following substances in order of their expected SN1 reactivity. A) CH3CH2Br B)CH2=CHCH3Br…

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Q: Br2 1. m-CPBA H*, H20 m-CPBA + HCI H2, Pt 5. + 2. 3. 4.

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Q: Please rank the below aromatics in order of increasing electron richness (least to most). OMe 2 NH₂…

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Q: Rank the organic halides in each group in order of increasing SN1 reactivity. Br Br Br Br b. Br a.

A: Nucleophilic substitution reaction is the one in which a nucleophile replaces the leaving group. So…

Q: Br Br Br II II IV

A: order of reactivity of alkyl halides in SN2 reactions is:  primary alkyl halide>secondry alkyl…

Q: Which of the alkyl halides below is ideal for a SN1 reaction? Br Br Br A B

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Q: Rank the organic halides in each group in order of increasing S2 reactivity. Br Br а. Br b. Br Br Br

A: Nucleophilic substitution reactions SN2 are those reactions in those reactions in which the rate of…

Q: 2. Explain the observed rate of reactivity of the following 2° alkyl halides in SN1 reaction. -Br Br…

A: The reactivity order of the given substrates can be well estimated by seeing the stability of the…

Q: Identify the SOMO of the photochemically-excited allyl anion. Options: А: y1 В: y2 С: y3 D: y4 E: y5

A: The molecular orbital in which a single atom is present is known as SOMO (singly occupied molecular…

Q: Which solvents favor Sy1 reactions and which favor SN2 reactions? a. CH,CH,OH b. CH,CN c. CH,COOH d.…

A: Protic solvent favors SN1 reactions while aprotic solvent favor SN2 reaction. (a) CH3CH2OH: it is a…

Q: Rank the following substances in order of their expected SN1 reactivity: Br Br CH3CH2B H2C=CHCHCH3…

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Q: CO2H HO2C

A: Diel-Alder Reaction: It is a 4+2 cycloaddition reaction between a diene and dienophile in thermal…

Q: CH3 CH3 OCH, H CHy CH CHs H CH, 3 2.

A: Solution :      Substituted rings are classified into two types on the basis of the type of…

Q: (+) i) Vs (+) В A ii) CF3 +) CF3 +) Vs H2N H2N A B

A: 1)

Q: Which of these compounds is MOST reactive towards NH₂? Select one: ов D O A OC

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

Q: Which of the following organic molecules has the highest Sn1 reactivity? Br Br Br Br

A: Here we have to choose the correct option about molecule which has highest SN1 reactivity and which…

Q: Which is the expected major product? OH OH CD pyridine ? OH (excess) OH CD3 D3C D3C OH OH OH ČD3 OH…

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

Q: Assign the structure of the following reaction taking into account regiochemistry and…

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Q: Br H;C. .CH3 `CH3 H

A: A<C<D<B This the order of decreasing reactivity for E2 elimination

Q: Identify compounds G and H in the following reaction scheme. Hrepresents the structure of…

A: The given chemical reaction is,

Q: rank the following compounds in order of their expected reactivity toward SN2 reaction CH3Br…

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Q: CH3 CH3ČCHCH3 CH3

A: The stability of the carbocation can be understood by the hyperconjugation structures. As the number…

Q: ) Explain the regiochemical outcome (i,e major vs minor product formation) for the following…

A: The mechanistic schemes for the first reaction is given below There are two path available to…

Q: Arrange the following compounds in the increasing order of reactivity towards Conc.HNO3 & Conc.H2SO4…

A: Reaction of these organic compounds with HNO3 and H2SO4 is electrophilic substitution reaction.…

Q: 3. Write the palladium-containing product for the following reaction and indicate its…

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Q: Rank the following organobromides in order of increasing rates of ionization to its carbocations and…

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Q: Arrange the following compounds in the increasing order of reactivity in SN' 1. CH3CH=CHCI 2.…

A: In SN1 reaction, the rate of reactivity increases with the increase in the stability of carbocation…

Q: Which of the following reagent/s will efficiently convert isopropylbenzene to 2- and…

A: Benzene is an aromatic compound and gives the different type of substitution reaction. These…

Q: Use the following molecule A to answer the questions below. CH3 CH3 (A) (i) Give the structure of…

A: Electrocyclic reaction in thermal condition and found out stereo.

Q: Which of the following compounds would you expect to bethe most generally reactive, and why? (Each…

A: Given compounds, cyclopropane, cyclobutane, and cyclopentane respectively.

Q: 4. For the following reactions, develop a transition-state structure using molecular models which…

A: All the transition states are given in third bracket. 4a) Reaction type: Electrocyclic reaction…

Q: Rank the following organobromides in order of increasing rates of ionization to its carbocations and…

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Q: H,O a) H,SO, Br2 b) H, с) Pt

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: Rank the molecules A to D shown below by decreasing reactivity towards iodo cyclohexane. H;C-CH,OH…

A: Correct option is 2 . B > A > C > D. B trifluoro ethanol is more acidic means more reactive…

Q: 4. Which of the following compounds is the least reactive dienophile in a Diels-Alder reaction?…

A: 4. Electron donating groups (Methyl group) decreases the reactivity of dienophile in Diels-Alder…

Q: CH3 OCH, CH3 H -CH3 CHs CH3 H CH3 3 4 1 2.

A: Here all molecules are carbocation . Thus carbo cations are stabilized by pushing electrons to that…

Q: what are the reagents to carry out this multi-step reaction and what are their inetermediates?…

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Q: Tell whether the following reaction is likely to be SN1, SN2, E1, E2 or E1cB, and predict the…

A: The given reaction is,

Q: 5. Which of the following is the correct order of increasing rate of bromination for the three…

A: The benzene ring acts as an electron-rich source. It undergoes an electrophilic addition reaction.…

Q: 1. What is the order of increasing reactivity in an SN1 reaction for these compounds? a to Br `Br II…

A: We can look at the mechanism for SN1 reaction to predict the reactivity.  At first the leaving group…

Q: 3. Rank the following carbocations in order of increasing stability (least stable to most stable) 1…

A: carbocation is a carbon with +ve charge, tertiary is more stable and primary is least stable.

Q: HO-CH2-CH2-Br CH3-CH2-CH2-Br I or II

A: Given compound HO-CH2-CH2-Br  CH3-CH2-CH2-Br