Draw the major organic product for the same substrate with two different conditions. NaOEt EtOН Нэс. CI (CH,), COK (сн, СОн CH 3

Q: Which statement best describes what is happening in step 6? (Remember, this is copied from the full…

A: In the given step left side one is imine. Imine is converted to examine  through tautomerisation

Q: A student wanted to know whether the greater proximity of the ucleophile to the C-2 carbon in the…

A: The reaction of HCl with 2-methyl-1,3-cyclohexadiene will form 1,2-addition product and 1,4-addition…

Q: For the dehydrohalogenation (E2) reaction shown, draw the major organic product, including…

A: Alkyl halides undergo E2 elimination in the presence of strong base, resulting in the formation of…

Q: Which of the following alkyl halides would be more reactive in an E2 elimination reaction?

A:

Q: Provide a plausible arrow pushing mechanism for the reaction below. Hint: NaOBr is in solution along…

A:

Q: How does the strength of the nucleophile affect an SN1 or SN2 mechanism?

A: Given reaction types,     SN1 reaction mechanism     SN2 reaction mechanism

Q: In the box to the left of each reaction below, write the mechanism by which it occurs (could be SN1,…

A: As per rule only three subparts can be answered.

Q: Write the complete mechanism with arrows of the following reaction. BI U Σ W A G

A: Pericyclic reaction occurs in presence of heat or light.

Q: what is the difference of the products in an E2 vs E1 reaction?

A:

Q: 5. Chauncy, an organic chemistry I class student, conducted the following dehydrohalogenation…

A: Elimination reaction :-        Reaction of alkyl halide with alcohol by strong heating gives mixture…

Q: Hepten-2-one is a ketone that also contains a C=C double bond between carbons 6 and 7. If this…

A: Alkene is reduced to give alkanes using Pt as a catalyst in presence of H2.

Q: Which statement best describes what is happening in step 5? (Remember, this is copied from the ful…

A: The reaction given is,

Q: Which of the following products is most likely to form in the greatest amount if the reaction shown…

A:

Q: Give the major elimination product for the following E2 reaction

A: E2 elimination reaction: It is a one-step reaction in which there will be a formation of an alkene…

Q: For each pair, predict the stronger nucleophile in the SN2 reaction (using an alcohol asthe…

A:

Q: Why do we not see 1,2-hydride shift rearrangements (or 1,2-methyl shift rearrangements) for E2…

A: A reaction which involve removal of a molecule containing atoms or groups give at least one p bond…

Q: Would you expect acetate ion (CH3CO2 -) to be a better nucleophile in an SN2 reaction with an alkyl…

A: The SN2/E2 reaction of alkyl halide is with neutral nucleophile/base, the increasing polarity of the…

Q: In a unimolecular elimination (E1) reaction, the correct order of mechanistic steps is А.…

A: E1 Mechanism Proceeds through loss of a eaving group (LG) and  then deprotonation.

Q: CH3 CH3 hv 12

A: In presence of hv and I2 , substrate molecule undergo electrocyclic reaction followed by…

Q: Fill in the boxes below with the necessary reagents. Each box must be one synthetic step (i.e., one…

A:

Q: For which reaction mechanisms—SN1, SN2, E1, or E2—of thefollowing statement true? A statement may be…

A: In substitution reactions, two mechanisms are, SN2 and SN1  . In elimination reactions, two…

Q: 0° CN is a nucleophile . hence it strong undergo SN2 Kh. CN CNO SN2

A: Both the anions undergo substitution reaction because both are good nucleophiles and good…

Q: a) If the following compound were to undergo an E2 elimination reaction, what would be the…

A: Given reaction:

Q: an instructor will demonstrate how quickly turpentine (paint thinner, a ~2:1 mixture of alpha and…

A: Given: (mix of Unimolecular Substitution and Elimination products)

Q: Would someone be able to draw the full mechanisms for these two reactions? Are these E1 or E2?

A: Would someone be able to draw the full mechanisms for these two reactions and Are these E1 or E2.

Q: 4. Complete the phrases with one or more of the following terms: Snl, Sn2, E1, E2. a) The reaction…

A: Points to remember: 1) SN1: Nucleophilic substitution reaction of first order SN2: Nucleophilic…

Q: 4. Study the curved arrows in the reactions below and provide the structures of the product(s)…

A:

Q: 4. Describe in table format the following criteria for S,' reactions: (a) strength of nucleophile;…

A: Following are the explanation for SN1 reaction according to given parameters.   Dear student, since…

Q: 10. (8pts each) Rank the reactivity toward the SN1 mechanism. Place answers in the box provided. CH₂…

A: Concept:  SN1 reaction: SN1 reactions are nucleophilic substitutions, involving a nucleophile…

Q: For the dehydrohalogenation (E2) reaction shown, draw the major organic product, including…

A: E2 reaction is a bimolecular elimination reaction to give an alkene. In the transition state, the…

Q: In both examples below the reactants shown are combined to bring about a nucleophilic substitution…

A: Benzyl bromide give bimolecular nucleophilic substitution reaction with NaCN in DMF solvent. The…

Q: 8. Rank from best (#1) to worst (#3) substrate in an SN2 reaction and explain. Br Br

A: When an incoming nucleophile attacks the alkyl halide and substitutes the halide ion and the rate of…

Q: For the dehydrohalogenation (E2) reaction shown, draw the major organic product, including…

A:

Q: Fill in the information based on the type of reaction mentioned in each column.  A. Draw the line…

A:

Q: Which is the best method for carrying out the following two-step transformation (as shown in…

A:

Q: From each pair, select the stronger nucleophile. Q.)Cl2 or I2 in methanol

A: Given: Cl- and I- in methanol.

Q: Which compound is a major product of the reaction sequence shown in the box? 1. EtO Na+ OEt 2. HСI,…

A:

Q: For the substitution (SN2) reaction below circle the nucleophile and draw a box around the…

A:

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

A:

Q: OCH, Br. CH,OH OCH3 1 2 3 Product 1 is made this way: Product 2 is made this way: Product 3 is made…

A: The reaction taking place is given as,

Q: If Zaitsev's rule does not apply and the base is bulky then how will the product look?

A: Bulky base like  potassium acetate will abstract beta proton from less hindered carbon to form less…

Q: The following reaction involves two sequential Heck reactions. Draw structural formu- las for each…

A: Given reaction,

Q: In the current experiment, we will use a different electrophile (the tert.-butyl cation) to alkylate…

A: In 1st step  to form tert butyl cation  Tert butyl alcohol react with acids to give tert butyl…

Q: How does changing the alkyl halide from CH3CH2Br to (CH3)2CHBr affect the rate of an E2 reaction?

A: The nucleophilic substitution reaction of an alkyl halide that involves both the concentration of…

Q: CHy O (+ 2cH,C00H) COOH Me Me

A:

Q: Can primary alkyl halides react by SN2, SN1, E2, and E1 mechanisms? Are any of these mechanisms…

A: SN2 reaction is second order nucleophilic substitution reaction that occurs in one step and SN1…

Q: 5) Show the complete mechanism for an E2 reaction with 1-bromo-2-tert-butylcyclohexane

A: Answer - 1-bromo-2-tert-butylcyclohexane - A chemical structure of a molecule includes the…

Q: CH3 CH3 СООН СООН NO2 ŠO3H ŠO3H Identify the reagents represented by the letters in the above…

A: Reaction involved following concepts 1) Fridel crafts alkylation 2) sulphonation 3) oxidation of…

Q: Identify the elimination product(s) formed in the reaction below. Br H,0 CH3 CH(CH,), O a. CH(CH,)2…

A:

Q: What is a mechanistic step for this reaction? Click on a letter A through D to answer. fuming H2SO4…

A: