CH3 + NaOH an alkene + NaCl + H,0

Q: 1) What is the major product of the following reactions? Remember to show stereochemistry where…

A: Given are organic reactions.Reaction a is hydrochlorination reaction. Reaction b is bromination…

Q: For the following reactions, give the major product(s) formed. Marks will be deducted for drawing…

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Q: Assign the appropriate stereochemistry to the following compound. (a) E Br. (b) z (c) R (d) S

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Q: Elimination occurs when (Z)-3-bromohex-3-ene is treated with NaNH2. Under the same conditions,…

A: The elimination reaction occurs when (Z)-3-bromohex-3-ene is treated with NaNH2 is as shown below.

Q: Draw the product of the following epoxide reaction, including the stereochemistry at any stereogenic…

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Q: Q12. (bremeetblbenzene 1 ydergeesan elimination following an E1 mechanism. Fill in the following…

A: E1 reaction occurs in two steps, step-1 is slow and the rate determining step that produces…

Q: Draw the structures of compounds A and B in the scheme below. Be sure to indicate the…

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Q: Consider the following reaction scheme:   (i) Identify compounds J and K. (ii) Draw a curved…

A: For the given conversion reaction, (i) identify compounds J and K. (ii) draw a curved arrow…

Q: (a) What alkene yields A and B when it is treated with Br2 in CCl4? (b) What alkene yields C and D…

A: A and B product is obtained from the trans form of Phenyl-2-propene.…

Q: Addition proceeds preferentially through the most stable carbocation intermediate. At high…

A: In this question, we will write the mechanism ( arrow pushing mechanism ) for the first step.

Q: None

A: First step is the rate determinins step.

Q: (а) но (b) -CH3 он (гасemic)

A: In this question, Reactants and Products are given and we used the Reagents to carried out this…

Q: 1) O3 A bicyclic Starting material H. 2) Мe>S H

A: The bicyclic material that would give the following product upon ozonolysis are as follows:

Q: 1. Draw the product of each of the following [3,3] sigmatropic rearrangements, including its…

A: Step 1:  Step 2:

Q: 4. The rearrangement reaction shown below was discovered in 1860. (a) Draw a mechanism for this…

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Q: the dehydrohalogenation (E2) reaction shown, draw the Zaitsev product, showing the stereochemistry…

A: According to zaitsev rule, highly substituted alkenes are formed as major product during the…

Q: Which of the following alkenes (a-c) reacts faster with HI?

A: Nucleophiles are nucleus loving species. Electrophiles are electron loving species. Carbocations are…

Q: Consider the following reaction scheme: (i) Identify compound E. (ii) Draw a curved arrow…

A: Radical cascade reaction.

Q: Predict the major mono-bromination products when the following compounds are brominated.

A: Monobromination product of alkanes of substituted alkanes can be obtained with the help of hv/Br2.…

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

A: E2 is a bimolecular reaction. The reaction involves one step mechanism in which the carbon –hydrogen…

Q: (a) CN 0 0 1. H₂O X, A 2. SOBг2, N 3.(CH3CH2)2CuLi; H₂O 4. NaBH4, CH3OH

A: The question is based on the concept of organic synthesis.We need to synthesize the product using…

Q: 5. Draw the mechanism and show the products with correct stereochemistry (a) OTS (b) Br OH + CH₂OH ?…

A: The objective is to complete the given reaction and find the product formed. Tertiary alkyl halides…

Q: A) Please provide a mechanism for the following transformations to the final product. 1) NaOEV EIOH…

A: As per our guidelines I  can answer only first question because you have posted multiple questions.…

Q: 7. Which substituent would be classified as a deactivating ortho/para director in an electrophilic…

A: In electrophilic aromatic substitution:Electron donating groups (EDG) are activating and ortho/para…

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A: Here we transform a alkene into a epoxides . That can be done by a oxidizing agent which a a extra o…

Q: 9. (a) Optically active 2-bromobutane undergoes racemization on treatment with a solution of KBr.…

A: a) Racemization is a process in which an optically active compound, which has different spatial…

Q: Predict the stereochemistry For the E2 reaction Draw a Newmann Projection Of the reactive con…

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Q: 9.63 For each of the following reactions, provide a complete, detailed mechanism and predict the…

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Draw the products (including the stereochemistry) formed in the following reaction.

A: Interpretation: The products formed in the following reaction is to be drawn including the…

Q: 3. Propose a mechanism and predict the product. Include any relevant stereochemistry. a) HCI b)…

A: a) Alkenes react with HCl and undergo addition reaction via carbocation formation mechanism. Since…

Q: Show how H may be converted into G and I. For both sequences, provide reagents and the structure and…

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Q: iii) iv) v) Br₂ EtOH Br2 0 °C Br₂, 1 eq

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

Q: Predict the major product of the following transformation: A) C) .CO₂Et H₂O* Heat COET C₁0H 100 B)…

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Q: 2. A. For the reagents listed below, draw the curved arrow mechanism to show the formation of the…

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Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.