A. Predict the major product of the reaction. Clearly indicate stereochemistry, if necessary. 1. NANH2 (excess) NH3/THF Br Br i-Pr 2. H3O* B. Draw a detailed arrow-pushing mechanism for the transformation, accounting for stereochemistry, if necessary.

Q: Explain why Jone's oxidation of 4-methyl-2-pentanol is faster than that of 3,3-dimethyl-2-pentanol.

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Q: Sl2, AICI; a complete curved mechanism -arrow generation of the active electophile 1. Two equivalent…

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Q: Draw the product of the attached reaction sequence, includingstereochemistry.

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A: The conversion of alkene into an alkane involves the reduction( addition of hydrogens).

Q: From each pair, select the stronger nucleophile. Q.) CH3OCH3 or CH3SCH3

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Q: Draw a detailed mechanism. For each step of the mechanism, jusiuny what you drew/explain the why…

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Q: Draw the products of the two step reaction sequence shown below. Use dash and/or wedge bonds to…

A: In this question, we have to draw the product of the step reaction sequence.

Q: Provide the missing starting material(s), reagents, or products for each reaction as indicated by…

A: All the missing starting material, reagents or products are given in a attached image.

Q: Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and…

A: Here I have shown a detailed mechanism of the reaction

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: CH;OH Br (solvolysis) Sn1 Sn2 E1 E2 Sn1 & E1 Sn2 & E2

A: The correct answer about above reaction mechanism is given below

Q: te a full mechanism for each reaction shown below. (I) Clearl (iii) show stereochemistry where…

A: According to our guideline, I can answer only the first three sub-parts.

Q: Draw a detailed mechanism showing the formation of the product, be sure to draw all intermediate and…

A: Radical Halogenation: In presence of light (hv) alkane with halogen reacts to form a halogenation…

Q: d. Draw the elimination product that would form upon reaction of (4S)-1-bromo-4- methylhexane with…

A: The reactant used is (4S)-1-bromo-4-methylhexane. The reagents used are (CH3)3COH and (CH3)3COK.

Q: (üi) from NH2 CH3

A: 3) The mechanism of formation of isoquinoline  has been outlined below

Q: a-Draw out detailed mechanisms for each reaction including electron pushing arrows, intermediates…

A:

Q: Which statement(s) is/are true regarding leaving Broups? L Weak bases make good leaving groups. II.…

A: I . ) Good leaving groups are weak bases. They're happy and stable on their own. Some examples of…

Q: (a) Draw the structure of molecule (A) that is in equilibrium with molecule (B). (b) Show a…

A:

Q: What reagent(s) will accomplish this conversion? EtLi followed by an acid wash O EtzSiCI followed by…

A: the given reaction is 1,4-addition to the alpha beta unsaturated ketone.  where the nucleophile is…

Q: Please provide a synthetic route for this molecule CH3 Ome

A: Synthetic route has been described.

Q: 4) Draw all mechanistic steps (initiation, propagation, termination) for the following…

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Q: Which is the best synthesis sequences, A or B, in Williamson ether synthesis? Explain your reasoning…

A: Bimolecular substitution reaction are generally faster for primary and slower for tertiary centre .…

Q: HN CH3B H,0 H* (cat)

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Q: ÇI NaSCH3 ? Be *very specific* about the stereochemistry of the product(s) of this reaction 18.

A: Given: Observing the given alkyl halide shows that it is a secondary alkyl halide with a good…

Q: H2O, H2SO4 H9SO4 A. В. С. E. None of these choices is correct. D.

A: In presence of HgSO4 and H2SO4 , H2O ,oxymercuration-demercuration reaction is carried out and…

Q: Show how a 1,2-shift forms a more stable carbocation from each intermediate.

A: The shift occurs in ionic species .and the shift males the carbocation more stable.  In 1st…

Q: HBr can be added to an alkene in the presence of peroxides (ROOR). What function does the peroxide…

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Q: Propose an efficient synthesis for the ff. transformations: b

A: a) Transformation 1 -

Q: major elimination product expected from the following reaction?

A:

Q: Propose a plausible mechanism using curved arrows that shows the 10. formation of product A only.…

A: The organic reactions are carried out in more than one step. It is carried out with the help of…

Q: NH2 CH3 OH Br CH3MG Br

A: Reaction 1: CH3OH acts as a base and abstracts the acidic proton from the amine. This PhNH- moiety…

Q: From each pair, select the stronger nucleophile. Q.)Cl- or I- in DMSO

A: The species, that make a covalent bond by donates a pair of electrons is known as nucleophile.…

Q: Draw an alkyl bromide with proper stereochemistry that can be used to synthesize the given alkene as…

A:

Q: Draw all stereoisomers that can be produced in this reaction. CH,N2 (excess) ? hv

A: Given,

Q: Br2 light or heat

A: Given reaction is :  Complete the reaction and gives the major product of the reaction = ?

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

A:

Q: if this react with (CH3)3CO- what is possible product and why sn1 reaction is not possible??…

A: The reaction does not follow the SN1 due to steric hindrance of tertiary butoxide so basically both…

Q: Draw the major product of the following reaction. Be sure to include stereochemistry if applicable.…

A:

Q: From each pair, select the stronger nucleophile. Q.) CH3SH or CH3S-

A: The species which make a covalent bond by donating a pair of electrons is termed as nucleophile.…

Q: Draw the products of attached reaction, and state whether the reaction is faster or slower than a…

A: The carbonyl group withdraws electron density from the ring deactivating it towards electrophilic…

Q: 3) Write a detailed mechanism of: CH CH. HNOT H'SO NO

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Q: What sequence of reagents would produce the folloing? (A) (B) (C) (D) 1. 2. Zn, HCI ??? AlCl3 CI,…

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Q: (üi) from Me NH2

A: The compound 2 can be prepared by Skraup synthesis of Quinoline

Q: What

A: We will write the product

Q: 3. For the following reactions A-C, please draw the products including stereochemistry where…

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Q: Find the diene and dienophile for the following product (retrosynthesis): ? + ? B B

A: Retrosynthesis: When Reaction  is carried out from product to Reactant side Then reaction is called…

Q: но, b) H

A:

Q: Rank the nucleophiles in each group in order of increasing nucleophilicity.a. -OH, -NH2, H2Ob. -OH,…

A: Nucleophilicity increases with increase in basicity of species.  Across a period from right to left…