I need fast answer.. Don't provide handwriting solutions.. Draw the structure(s) of the major organic product(s) of the following reaction.CH3+THF-78°If no reaction occurs, draw the organic starting material.Draw enolates in their carbanion form.Include counter-ions, e.g., Na*, I, in your submission, but draw them in their own separate sketcher.• For multi-step processes, draw the product(s) of the last step.N.[F

Product of following reaction can be made by applying appropriate reaction mechanism.

Answered: Draw the structure(s) of the major…

Draw the structure(s) of the major organic product(s) of the following reaction. CH3 + THF -78° If no reaction occurs, draw the organic starting material.

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter20: Nucleophilic Substitution Reactions: Competing Nucleophiles

Section: Chapter Questions

Problem 2Q

See similar textbooks

Related questions

Q: A student wants to investigate the strength of intermolecular forces of different materials. She has…

A: Intermolecular forces are responsible for adhering molecules to each other. Surface tension is…

Q: 8. Determine the number of CH₂Cl2 molecules in 42.463 g of CH₂Cl₂. The molar mass of CH₂Cl2 is…

A: Avagadro's law states that 1.0 mole of any substance Avagadro number () of species.Number of moles =…

Q: CH,F and then determine if the molecule is polar or nonpolar.

A: In the lewis structure of a molecule, a covalent bond is represented by a line and unpaired…

Q: The Sharpless epoxidation is used when a single enantiomer product is required. Predict the…

A: The given reaction is Sharpless asymmetric epoxidation reaction.The Sharpless asymmetric epoxidation…

Q: 7. For the following species dissolved in water, at 298 K: (1) Na* ion (D in H:0 = 1.33 x 10° m²…

A: Diffusion of solute in water

Q: Please don't provide handwriting solutions...

A: The objective of this question is to understand the reaction mechanism of…

Q: Complete and balance the acid/base reaction. Hl(aq) + KOH(ag) What is the sum of ALL the…

Q: ra mple 2,13 regioselectivity of the reaction of Br, with alkanes. CH3 → Monobromoalkanes + HBr heat…

Q: Provide a complete organic synthesis showing all the correct electron-arrow pushing mechanism for…

A: Iso butyl aluminium hydride is a reducing agent it reduces unhydride to aldehyde.In the second step…

Q: Nitrogen-13 is used in tracers injected into the bloodstream for positron emission tomography (PET).…

A: Answer:Since, all nuclear reactions are first order reaction, therefore integrated rate law for…

Q: Draw the Lewis structure of Oz and then determine if the molecule is polar or nonpolar.

A: The Lewis structure of the O2 molecule is shown below: The atomic number of oxygen is 8. There are 6…

Q: The following transformation will require the use of a blocking group. H₂N. True O False NH2 H₂N NO₂…

A: Given statement: The following transformation will require the use of a blocking group.We have to…

Q: Draw the product of this reaction. Ignore inorganic byproducts. Br2 (2 equiv) Drawing Q

A: In the reaction given above, reaction between alkyne and bromine (Br2) is given. In this reaction,…

Q: 12. If we have 9.92 g of phosphorus, P4, and an excess of sulfur, S8, what mass of P2S5, in grams,…

A: The mass of P4 given is 9.92 g.The given balanced chemical equation is .To find the mass of P2S5.To…

Q: re of carbon monoxide and water vapor. At high temperature synthesis gas will form carbon s hydrogen…

A: The reaction is as follows - CO + H2O -----------------> CO2 + H2 I 1.6 4.5…

Q: 1. Lead ions can be precipitated from aqueous solutions by the addition of aqueous iodide. Below is…

A: The balanced net ionic equation will be:

Q: The following reaction was performed in a sealed vessel at 729 °C: H2(g) + 12(g) 2HI(g) Initially,…

A: First write down the ICE table of reactions. From that calculate the change in concentration and use…

Q: consider the equilibrium NO2(g) NO(g) +1/202(g). One mole of TO2(g) is placed in a vessel and…

A: The objective of the question is to determine the standard Gibbs free energy and standard enthalpy…

Q: Problem 3. Design a synthetic sequence that accomplishes the following transformations. Include…

A: Given are organic reactions. In reaction a, alcohol is converted into alkene. In reaction b, alkene…

Q: Draw the products of this reaction. Use a dash or wedge bond to indicate stereochemistry of…

A: To draw the product for the reaction of given alkene which is treated with OsO4 and NMO. We have to…

Q: A chemist designs a galvanic cell that uses these two half-reactions: half-reaction 2 H₂O()+2e 1…

A: Since you have asked multiparts, we will solve the first three subparts for you. If you want any…

Q: dont proide handwriting solution ....

A: Approach to solving the question:Detailed explanation: Examples: Key references:

Q: 12B.1 (a) Write down the expression for the partition func- tion of a molecule that has three energy…

A: (a) Write down the expression for the partition function of a molecule that has three energy levels…

Q: Which diatomic molecule has the smallest dipole moment? A) F2 B) O2 C) N2 D) H2 E) All equal

A: Dipole moment is the measurement of polarity of each bond inside a molecule and polarity of bonds in…

Q: How would you achieve the following transformations?Á COOH (zig E) Ssansupes nostot

A: Given is organic reaction. The given reactant is benzene.The given product is 2-phenylpropionic…

Q: CH3 H3C-C H3C

A: While numbering ring is given priority. As ring contains double bond . Substitutituent is at 4th…

Q: Predict whether or not a precipitate forms if you mix 75.0 mL of a NaOH solution with pOH = 2.60…

A: If the ionic product(Qsp) of a compound overcomes its solubility product constant(Ksp) then a…

Q: Calculate the pH during the titration of 30.00 mL of 0.1000 M KOH with 0.1000 M HBr solution after…

Q: OH Ph Pdll (Cat.) -Ph

A: Given:Pd( II) acts as a catalyst.Palladium( II) (Pd( II)) is a commonly used catalyst in various…

Q: 6. What product would you obtain from catalytic hydrogenation of the following alkene? HO Show…

A: Syn addition of H2 take place

Q: Suggest readily available starting materials and reaction conditions suitable for obtaining each of…

Q: The proton with the lowest delta value (the most shielded) is The proton with the highest delta…

A: The NMR spectroscopy is an abbreviated form of Nuclear Magnetic Resonance Spectroscopy. Each kind of…

Q: A certain half-reaction has a standard reduction potential Ered = -1.01 V. An engineer proposes…

A: It is given that E°cell ≥ 1.00 Since, at least word is written .at least means minimum value.E°cat…

Q: In the formation of copper(11) oxide from copper(1) hydroxide mixture, what do we need to do to…

A: We have to tell the formation of copper (II) oxide from the copper (II) hydroxide mixture. The given…

Q: Classify each reaction as oxidation, reduction, or neither. OH

A: In organic chemistry , if the product is gaining hydrogen or oxygen is being lost , it is said to be…

Q: er, answer the following question. 128 grams of KBr, and combine it, in a , with water at a…

A: From the graph , At 60 °c, The solubility of KBr is 86 g KBr/100 g water

Q: For the reaction H₂(g) + Cl₂ (9)→ 2HCl(g) AG=-192 kJ and AS=20.0 J/K at 347 K and 1 atm. This…

Concept explainers

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.

Question

I need fast answer..

Don't provide handwriting solutions..

Draw the structure(s) of the major organic product(s) of the following reaction.
CH3
+
THF
-78°
If no reaction occurs, draw the organic starting material.
Draw enolates in their carbanion form.
Include counter-ions, e.g., Na*, I, in your submission, but draw them in their own separate sketcher.
• For multi-step processes, draw the product(s) of the last step.
N
.
[F

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1: Step 1

VIEW

Step 2: Step 2

VIEW

Solution

VIEW

Step by step

Solved in 3 steps with 1 images

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

#8).
Draw the structure of the major organic product of the following reaction. Predict whether the product will be an aldol or an enone. CH3 CH3 NH ? 95% aq. ethanol, 25⁰ You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • If no reaction occurs, draw the organic starting material.
Can someone show me the complete mechanism with arrows? How would the reaction be different if no heat was added?
Indicate the correct set of reactions from the choices below that would accomplish the following synthesis MOST efficiently (Hint: what is the MAJOR product of each step). (+ enantiomer) Product Starting Material O1. MeMgBr then HCI, 2. H2SO4, heat, 3. NBS, peroxide, heat O1. H,SO4. MEOH, 2. POCI3, pyridine, 3. HBr, CH,00CH3, heat O1. MeMgBr then HCI, 2. H,SO4, heat, 2. HBr, peroxide, light O1. Meli then H,0, 2. TSCI, pyridine 3. NaBr (excess), heat O1. LIAIH4 then H20, 2. H,SO4, heat, 3. HBr
It will be helpful if I find the distinction between these two products since they are both Elimination reactions? Will one proceed via E1 or E2? If so, why is that the case?
#8).
9. Identify the major product of each reaction and indicate whether the reaction is likely to proceed by a bimolecular (SN2) or a unimolecular (SN1) mechanism. Why is each reaction likely to proceed via the mechanism you have chosen? (Hint: The leaving groups -OSO2CF3 and -OMs are also sulfonates (like tosylate, -OTS), so they are also good leaving groups.) a) b) d) Oso₂CF, OMs Br Nal acetone NaCN DMF CH₂OH 80% H₂O, 20% ethanol -6-
2. Given the following sequence of reactions, draw the structure of products A and B and write a detailed reaction mechanism that explains their formation. H2N H30* A B 3. Write a detailed reaction mechanism for the following transformation. Upload your answer as an attachment. OEt OEt OE
Please don't provide handwritten solution ..
Ba 07.
Give the major organic product(s) for a step of the following sequence of reaction. Write NR if the reaction will not occur.
H₂O N(CH3)2 H₂SO a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. You do not have to consider stereochemistry. Do not include counter-ions, e.g., Na", I, in your answer. In cases where there is more than one answer, just draw one. Q 6 QQ 4 ChemDoodle b. Draw the structures of the organic products of the acyl transfer reaction.