Would Be the Alkyl halide and nucleophile to prepare SN1 mechanism? what the following structure By an PH Alkyl halide nucleophile

Q: What change would you expect on the rate of the Sy2 reaction of 1-lodo-2methylbutane with cyanide…

A: The rate of the SN2 reaction of 1-iodo-2-methylbutane with cyanide ion remains unchanged  if the…

Q: Through what basic mechanism is 1-methylcyclohexanol converted to 1-brom methylcyclohexane upon…

A: Basic mechanism is 1-methylcyclohexanol converted to 1-bromo-1- methylcyclohexane upon treatment…

Q: 15. Which of the following correctly describes the relative nucleophilicities of methoxide and tert-…

A: Nucleophilicity is defined as the ease of donation of electrons by the electron rich species to the…

Q: Which of the following Halides will not function as an electrophile in a friends-craft reaction?

A: In Friedal-crafts alkylation reaction, an incoming electrophile attacks an aromatic system and the…

Q: Trimethylphosphine is a stronger nucleophile than triphenylphosphine, but it is rarely usedto make…

A: Given data :   Trimethylphosphine is a stronger nucleophile than triphenylphosphine, but it is…

Q: is

A: In SN1 and E1 reaction polar protic solvent is used such as alcohol and acid.generally polar protic…

Q: Which is the strongest nucleophile in a polar aprotic solvent, such as acetone? O CH3ONa O CF3ONa O…

A: Nucleophile, is an atom or molecule that in chemical reaction seeks a positive centre, such as the…

Q: The compound below can be prepared with an alkyl iodide and a suitable nucleophile. Identify the…

A: The given structure of the compound appears as follows:The structural formula of the above compound…

Q: OSO₂CF To NUO CH₂CH₂OH Pamer b) Clº Nu "Triflate" is a good leaving group "Triflate"-oso,CF> Fo…

A: In SN1 reaction polar protic solvent is used.in this reaction polar protic solvent is used so…

Q: enolate base enolate base

A: The first compound contains an active methylene group. The alpha proton carbonyl group is acidic in…

Q: In Friedel-Crafts acylation, why is water needed? Why does the entire step 4 mechanism need to…

A: We have to explain the role of water in Friedel-Crafts acylation product. Also, we have to give the…

Q: Which of the following is expected to be most reactive towards a nucleophilic aromatic substitution…

A: We have to tell which compound is more reactive towards a nucleophilic aromatic substitution via the…

Q: bJ HCl, traue peroxides

A: Which of these is the best reagent to affect the transformation? (a) HCl (b) HCl, peroxides (c)…

Q: Indicate an alkyl halide with an appropriate choice of leaving group and the nucleophile that would…

A: Answer:S in sn1 is for substitution reaction, n is for nucleophilic and 1 is for unimolecular, so,…

Q: Sort in increasing order of reaction rate against electrophilic aromatic substitution:…

A: Step 1: Step 2: Step 3: Step 4:

Q: Which of the following is NOT a correct statement about the electrophilic aromatic substitution…

A: The incorrect statement about the aromatic electrophilic substitution has to be given.

Q: Ph * Ph Bv 014 Br CN Ph. with

A: Applying concept of organic synthesis and reaction mechanism.

Q: Which of the following is the strongest nucleophile? OH- H20 H2S HS-

A: Answer :-  HS-  -------------------------------------

Q: Internal alkynes are able to selectively form one product when subjected to most reaction…

A: Alkynes are unsaturated hydrocarbons that can carry out electrophilic addition reaction by…

Q: Draw a mechanism for the nucleophilic acyl substitution/addition reaction with LiAlH4. Why doesn't…

A:

Q: If a solvent more polar than ethanol were used would you expect the SN1 reaction rate to increase or…

A:

Q: Why are NH3 and CH3NH2 no longer nucleophiles when they are protonated?

A: A molecule is said to be nucleophiles when it donates its lone pairs of electrons.  In protonation,…

Q: 11) The SN2 reaction of iodocyclopropane with sodium methylmercaptide (CH3SNG) is not observed. Why?…

A: In transition state (T.S) of SN2  some positive charge is formed .

Q: None

A: