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What determines a compounds reactivity in an SN2 reaction?
Stearic hindrance and stability of carbonium ion, less stearic hindrance and less stability of carbonium ion favors the SN2 reaction.
Why do secondary haloalkanes (like 3-chloropentane) give poor yields with the Williamson ether synthesis?
Because they have been reacted with primary sulfonate under typical SN2 condition.
Which is more oxidized Sn2 or Sn plus 4?
Sn4+ is fully oxidised, Sn2+ only half
What is the symbol for tin 2 electrons lost?
This symbol is Sn2+.
What is the role of solvent in nucleophilic substitution reactions?
in sn1 reactions polar solvents are used.why b coz, polar solvent stabilise the intermediate which is formed in the reaction.but in sn2 reactions non polar solvents are used.in this reaction intermediate is not formed.
What type of reaction does Sn2 Sn4 represent?
Oxidation!
What determines a compounds reactivity in an SN2 reaction?
Stearic hindrance and stability of carbonium ion, less stearic hindrance and less stability of carbonium ion favors the SN2 reaction.
What is an SN2 reaction in organic chemistry?
An SN2 reaction is a one step bimolecular substitution mechanism which is 2nd order in kinetics. An electron rich species (called a nucleophile) attacks an electrophile (electron deficient species) while a leaving group (LG) leaves. Typically a good nucleophile for an SN2 reaction are halides and moderate to strong bases. Good leaving groups are species that are stable on their own like halides, water, tosylate, and protonated ethers. Conditions for an SN2 reaction are similar to the conditions necessary for an E2 elimination reaction; the two are in constant competition.
How can a Chiral Carbon be formed?
A chiral carbon is bonded to four different substituents. -------------------------------------------------------------------- Yes I know that but how...do u know the mechanism ??? I am also confused by your question... Any reaction that yields a carbon with 4 different substituentes will yield a chiral center. There are reactions that can create certain isomers, S or R. Is that what you are asking? If so, there are many hundreds of these reactions. Are you maybe referring to an inversion of chirality, such as an SN2 type reaction? yes the SN2 mechanism please can u explain it further more....
Why is bromocyclopentane more reactive than bromocyclohexane when heated with sodium iodide?
This follows a Sn2 reaction.
Why do secondary haloalkanes (like 3-chloropentane) give poor yields with the Williamson ether synthesis?
Because they have been reacted with primary sulfonate under typical SN2 condition.
What is the difference between SN1 and SN2 reactions?
An SN1 reaction is an unimolecular substitution reaction (hence the name SN1). This means it's a substitution reaction in which the rate of the reaction is only dependent on the concentration of the substrate, as opposed to SN2. In an SN1 reaction, the leaving group of the substrate departs first, leaving a carbocation on the substrate. Then, the nucleophile donates an electron pair to the carbocation and forms a bond. In an SN1 reaction, the carbon molecule bonded to the leaving group must therefore be a tertiary substituted carbon. This is because when the leaving group departs from the molecule, only a tertiary substituted carbon is stable enough as a cation. Keep in mind that an SN1 reaction leads to two isomer products. If the tertiary carbon is a chiral senter, the two products of the SN1 reaction have an R and S configuration, respectively. The mixture of these isomers is racemic, and the isomers have identical physical properties.
Why is ether medium used in wurtz reaction?
Wurtz reaction is a SN2 reaction and thus requires an aprotic solvent as it medium. dry ether proves to be a very good, non-polar, aprotic solvent and is thus used in Wurtz reaction.
Which is more oxidized Sn2 or Sn plus 4?
Sn4+ is fully oxidised, Sn2+ only half
What is difference between SN1 and SN2 reaction?
An SN1 reaction will occur if:The substrate can form a relatively stable carbocation (typically from a tertiary carbon)The nucleophile is relatively weakA polar protic solvent is used.An SN2 reaction will occur if:The substrate is with a relatively unhindered leaving group (typically from a methyl, primary, or secondary alkyl halide)The nucleophile is strong (usually negatively charged) and is of high concentrationThe solvent used is polar and aprotic.
What would be the effect of carrying out the sodium iodide in acetone reaction with the alkyhalides using an iodide solution half as concentrated?
A reaction with alkyl halides in NaI with acetone is by the Sn2 mechanism. The rate for an Sn2 mechanism is directly proportional to the concentration of the nucleophile: rate = k[nucleophile][alkylhalide] If the iodine solution (the nucleophile) is half as concentrated, then the rate will also be halved. rate = k [nucleophile]/2 [alkyl halide]
Mechanism of nBuBr plus KCN------nBuCN?
The given reaction is:The given reaction is an SN2 reaction. In this reaction, CN−acts as the nucleophile and attacks the carbon atom to which Br is attached. CN−ion is an ambident nucleophile and can attack through both C and N. In this case, it attacks through the C-atom.
