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A: In organic chemistry, several kinds of reactions can take place on alkene. Alkene is an…
Q: Rank the following nucleophiles in order from slowest SN2 reaction rate to fastest if DMSO is the…
A: Given nucleophiles are;
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A: Reaction goes via SN1 mechanism because losing Br- it becomes tertiary carbocation .
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A: The initiation step in the peroxide promoted addition of HBr to an alkene is the homolytic cleavage…
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A: According to our guideline, I can answer only the first three sub-parts.
Q: :O: :CEN CN
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Q: Draw the products of attached reaction and indicate their stereochemistry.
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Q: Draw all resonance structure contributors that result from ortho position of the nucleophile. Raw aL…
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Q: Draw the structure(s) of the major arganic product(3) of the following reaction ci CugO/Cu(NO3)2 in…
A: This is an example of Sandmayer reaction
Q: Diagram the mechanism of the reaction and draw the product(s): Br + AIBT3
A: This reaction is electrophilic substitution..
Q: OH Br
A: 1-> elimination of leaving group. 2-> base can abstract most acidic hydrogen.
Q: e ASOho anoluloe oodheTVbu oe 29.Draw a detailed free energy diagram for the following E1 reaction.…
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Q: CI NaSCH3 18. Be *very specific* about the stereochemistry of the product(s) of this reaction
A: Since you have posted multiple questions, we are entitled to answer the first only.
Q: An alkyl halide was reacted with sodium cyanide in ether. Drag and drop each part of the SN2…
A: the reaction of an alkyl halide with sodium cyanide is an SN2 mechanism and product is formed with…
Q: Rate the below nucleophiles in terms of INCREASING nucleophilicity. Explain why. CH3OH CH;0 t-BuO-…
A: As the name suggests, nucleophiles are those reagents that possess attraction for the positively…
Q: Choose which compound is more reactive when reacted with NaOH in water solvent and ne reason…
A: The compounds given are carboxylic acids. And the reaction is taking place with base NaOH.
Q: What are the possible constitutional isomers and rank by SN2 reaction.
A: Isomers are the compounds having same molecular formula but different structure. The phenomenon…
Q: Identify the minor elimination product in the reaction below. H,O A а. Ob.
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Q: CHa Br, FeBr, NHCOCH, heat H3C CH, SO,, H-SO, Br CF3 heat
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Q: Which of the following will react most slowly with cyanide nucleophile (NC-) in an Syl reaction?…
A: SN1 stands for the unimolecular nucleophilic substitution reaction It takes place in 2 steps The…
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A: The complete reactions are shown as follows:
Q: Rank the following nucleophiles (Nu) in order of increasing reaction rate in an SN2 reaction (from…
A: The rate of SN2 reaction will directly depends on the strong nucleophilicity of nucleophiles.
Q: Draw the substitution product(s) of the following reaction and show the mechanism by drawing the…
A: The products are
Q: Determine the mechanism of nucleophilic substitution of attached reactionand draw the products,…
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A: The species, that make a covalent bond by donates a pair of electrons is known as nucleophile.…
Q: Consider the following alcohols: С. ОН A. В. D. LOH ОН Which can form a rearranged carbocation…
A:
Q: Consider the reaction below to questional 29. The mechanism of this reaction is: b. S haver the…
A: There are multiple questions. We are authorised to solve only one question at a time. Please post…
Q: ank the carbo OlUlI 3. Each of the carbocations below will spontane rezIrangement product.
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Q: -phenyl- ga) al with the the final Intermediates Draw sequence below along reaction after each step…
A: The crucial intermediate for this given reaction sequence is a carbanion and it reacts with given…
Q: Find the products (A and B) for the following reaction sequence: Br NaOEt, E1OH Brz, light B.
A: NaOEt act as a base and abstracts the proton results in the formation of alkene(A) by E2 mechanism.…
Q: Determine the mechanism of nucleophilic substitution of attached reactionand draw the products,…
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Q: For the reaction below: CI a Draw the organic product(s). AICI3
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Q: Draw the product of the reaction below including stereochemistry. CH3ONA HI
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Q: alkyl halde The mechanism of this reaction is SN (SN2 or Sy1?). Explanation: Jvcleophile
A: SN2 reactions occur in a single step whereas SN1 reactions are those that occur in 2 steps. SN2…
Q: Draw the major organic substitution product(s) for (2R,3S)-2-bromo-3-methylpentane reacting with the…
A: Step 1: Here, in the given reaction, the given nucleaophile is an ethoxide CH3CH2O-. The ethoxides…
Q: Consider the following alkyl chlorides: CI ĆI А. С. Which will MOST easily form a carbocation…
A: We know that most easily form a carbocation intermediate of that alkyl chloride which form stable…
Q: Draw the most likely products of each reaction. d. Predict which reaction will be faster. e. Draw an…
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Q: In the E1 reaction, how is the rate affected when the concentration of attacking nucleophile is…
A: The rate of a reaction helps in the determination of the effect of the change in the concentration…
Q: Na :CEN: CI acetone, 25 °C
A: SN1 is the 1st order substitution reaction whereas SN2 is the 2nd order substitution reaction. In…
Q: Consider the addition reaction below. In the box A, draw the strucutre of the electrophile involved…
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Q: Which of the following substrates will have the fastest rate of reaction with NaCN in DMSO? O A) B)…
A: Given: Alkyl halide + NaCN in polar aprotic solvent DMSO
Q: Vhat is/are the missing reagent(s) "A" in the following reaction? HO ???? ОН NazCr204/H* O All of…
A: ->K2Cr2O7/H^+ and KMnO4 are strong reagent it oxidize alcohol to carboxylic acid.
Q: O Consider the nueleophilic subst itutión reaction of methanol with 2-bromobutane, a) Is this mostly…
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Q: hich alkyl halide will have the slowest rate when reacting with sodium methoxide? O O F CI
A: Alkyl halides are the organic compounds in which halogen group is attached to carbon atom.
Q: 1. Rank the following nucleophiles in order from slowest S2 reaction rate to fastest if DMSO is the…
A: Introduction : SN2 reaction is Nucleophilic substitution reaction 2 which attacks the substrate and…
Q: Draw the Product(s) and the Step-by-Step Mechanism for the Reactions Shown. Make sure to indicate…
A: the reaction and mechanism are as follows:
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- Plastic photochromic sunglasses are based on the following reversible rearrangement of a dye inside the lenses that occurs when the lenses are exposed to sunlight. The original dye absorbs UV light but not visible light and is thus colorless, while the rearrangement product absorbs visible light and is thus darkened. (a) Show the mechanism of the rearrangement. (b) Why does the rearrangement product absorb at a longer wavelength (visible light) than the original dye (UV)?14) what type of chemicall reaction in the follasing example? is illustrated so Ca)キ cambination reaction decomposi tion reaction Single-veplacement reactian noutralizathon reactionn double -ement reactian replace! ( plz ans with proper explanation , aslo give mechanism
- write the magor producb formed by the to llow ung eaction, Assume that You have enough of each rea Reactant to dvive the veaction bo Completion. Assume bhet thore i's protic wek up alone as neee ssary agont/ clPlease 'Explain the mechanisms/steps taken in arder to2or he productb) Identify A and B and provide mechanism of the reaction. NH2 HONO heat A `CO2H H;CO,C
- 24. Which product is formed by the reaction ? A) | B) || C) ||| D) IV Br ОН NaH Br ... هستم IV1) A cataly st function by a Lowenng the energy of the react ants the energ y of the products reacti on C. Prosidina df Providing Ja reacti on energy: ' path with a lower activation enevay path with a a reach on higher acti vationH OTS Naten DMSO Crive the mechanism and include Stereochemistry when athe appropriate. Ho
- For the following reaction: Explain how to decide which mechanism(s) the reaction will follow including information about: o alkyl halide substitution (what type and what this tells you about the preferred mechanism) o nucleophile or base strength o solvent (what type and how this affects the mechanism) State which mechanism(s) will occur.". Draw the mechanism. Draw the product(s). *How can you distinguish in a SNAr reactionwhether it will occur according to an addition- elimination or an elimination-addition mechanism?Draw a plausible mechanism for the reaction shown below. Et Ме OH ..Me 1) Excess EtMgBr 2) Hо Et "CI