Question

show de ne yapmetnim that could certain de omnis afect of de hallowing moderne from the mention Show the step by step mechani

0 0
Add a comment Improve this question Transcribed image text
Answer #1

These 4 products can be formed by SN1 and E1 reaction.

Let's name the 4 products as a, b, c and d.

BR AD11 VI (product-a) (prescent-b) (proderet-f) (producta)

Product a and b can be formed by SN1 reaction, SN1 means unimolecular substitution reaction. Following is the mechanism,

BROK o Sul reaction, frrest generates a carbocation.

So, in the first step of the SN1 a carbocation is generated. Carbocations are planar in nature. So, the other reagent can attack the carbocation from either above the plane or bellow the plane.

Formation of product-a: (attack from above the plane)

attack from above the plane This group stays above the plane because of the attack from above the plane) (compound-a) )))))

As we can see attack from above the plane gives rise to "product-a".

Formation of product-b: (Attack from bellow the plane)

BR: (attack from bellow the plane) DON This group stays bellow the plane because of the attack from bellow the plane.) (produ

As we can see attack from bellow the plane gives rise to "product-b".

This molecule can undergo E1 reaction too. E1 reaction means Unimolecular elimination reaction. In E1 reaction the alcohol attacks the hydrogen molecule adjacent to the carbocation and gives rise to a double bond. There are two adjacent hydrogens to the carbocation so, two types of double bonds are possible. Following is the mechanism.

A Two types of hydrogens adjacent to the carbocation. VINN

Formation of Product-C:

(product-C)

Formation of Product-d:

(product-d)

Add a comment
Know the answer?
Add Answer to:
show de ne yapmetnim that could certain de omnis afect of de hallowing moderne from the...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • 20 points show the mechanism of the formation of Alcohol A from me hyration of 2-motor-ne. Start by owing the react...

    20 points show the mechanism of the formation of Alcohol A from me hyration of 2-motor-ne. Start by owing the reaction of Howth S to generate the strophile Use that clectrope to complete the mechanism in the second box. Make The two mechanism in the proper ces below Show the movement of electrons wing curved arrows Show allone pair and formal charge . Do not add any other reagent or solvent C 94 os . 4-6-09 for the formation of...

  • Most reactions occur by a series of steps. The energy profile for a certain reaction that...

    Most reactions occur by a series of steps. The energy profile for a certain reaction that proceeds by a two-step mechanism is shown below. 2 1 Reaction coordinate In regard to the energy profile, identify the following. (a) The positions of reactants and products reaction coordinate for reactants 1 reaction coordinate for products 3 (b) The activation energy for the overall reaction. (Enter your answers in increasing numerical order.) the energy difference between reaction coordinatesSelect and-Select (c) AE for the...

  • Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1:...

    Show lone pairs on all appropriate atoms and the proper flow of electrons. (1) Mechanism #1: • Predict the products of the following reaction under different temperature conditions. • Show the mechanism for how the two products are formed at different temperatures (include resonance structures if appropriate). • Label the kinetic product and the thermodynamic product. (5 points) -80 °C + HBr 40 °C (2) Predict the product and show the complete mechanism for the following reaction. • Make sure...

  • 1. Provide the missing conditions for both steps and show how the amide can be converted...

    1. Provide the missing conditions for both steps and show how the amide can be converted to the corresponding acid chloride. Step 1 Step 2 Step 1 Conditions for step 1 (brain-twister: is there just one way?): Conditions for step 2 (same brain-twister): Full reaction scheme: 2. Consider the following reaction: 1. NaOM/MeOH 2. H,0* Does it have a specific name? How many products are possible? Show all of them. Suggest a synthetic route that leads to a lesser number...

  • need Help! I don't even know where to start. if you could please show every step...

    need Help! I don't even know where to start. if you could please show every step and maybe explain why you did it. thank you! C. Provide detailed mechanism for the product provided. Draw 4 other possible products at the bottom NaOH, H20 heat + other products

  • Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of...

    Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of 2,2,4,4-tetramethylpentane with chlorine in light. Map Complete the multistep mechanism for the formation of each of the possible monochlorination products from reaction of 2,2,4,4-tetramethylpentane with chlorine in light. Initiation step in the presence of light. Use curved arrows to show the mechanism of the propagation steps below. (Click on the blue box to toggle through four possible arrow choices.) a) Formation of the...

  • Could you please help and answer this question by drawing the mechanism for the reaction and...

    Could you please help and answer this question by drawing the mechanism for the reaction and show a possible reaction condition that would allow the product to be the only one forming? If you can explain how and why that would be greatly appreciated. Thank you!! 4. In place of the written protocol show the mechanism of the following reaction and determine how many products can form. Indicate the full mechanism for ONE product formation but show all potential final...

  • Show by a series of reactions how you could prepare the following products from the indicated...

    Show by a series of reactions how you could prepare the following products from the indicated starting compound. Please, be sure to clearly indicate the reagents used in each step. Draw all intermediates a) 4pts used cyclohexanol as your starting materials. Освен -CECH from -OH b) 4pts Y c) 2pts

  • Could you please help and draw this mechanism? Thank you! 3. Ille meeldiSM UI we ledCLIUI....

    Could you please help and draw this mechanism? Thank you! 3. Ille meeldiSM UI we ledCLIUI. 4. In place of the written protocol show the mechanism of the following reaction and determine how many products can form. Indicate the full mechanism for ONE product formation but show all potential final products that can occur. Reactions must be hand-drawn! KH ethanol

  • 1) Predict the major product in each of the following transformations. Show the mechanism. 2) Show...

    1) Predict the major product in each of the following transformations. Show the mechanism. 2) Show how you could synthesize the products below using a Grignard reagent and appropriate electrophile by drawing the overall balanced equation. Include the mechanism. Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,сн,МgBr (еxcess) 2. HС{aq) 1. PhMgBr (1 equiv.) 2. HCI(aq) ОН HO 1. CH2MgBr (2 equiv.) 2. HCl(aq) Н Show how...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT