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When achiral starting materials yield a product that contains a chiral center the product will be?
racemic mixture
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.
What kind of reaction -SN1 or SN2 or E1 or E2- is expected for secondary haloalkanes with sterically hindered strong bases?
the mostly undergo SN1 or E1.. but ratio of E1 is higher...
What type of reaction is the hydrolysis of t butyl chloride?
SN1 reaction
What is steric acceleration?
For Sn1 reaction the rate usually increases due to steric acceleration. For example the more methyl groups a compound has i.e the more tertiary it is the faster the rate of reaction will be for an Sn1 reaction.
When achiral starting materials yield a product that contains a chiral center the product will be?
racemic mixture
What is the modification of an existing product or process?
Innovation is the modification of an existing product or process.
What is an example of a market modification?
market modification can be done by product modification, i.e the promotion of SUNSILK has increased the market share by including a bit modification in their product and adding a factor of dermotologist. actually market modification is the modification in market share.
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.
What is sn1?
Spare No 1
What does the product modification strategy of international marketing entail?
A product modification strategy keeps the physical product essentially the same; modifications, however, are made to meet local conditions or preference in package sizes or colors
How do you modify products?
A modification of a product is a change in that product. Usually an improvement in the use or manufacturing process.
What is the difference between an E1 and a Sn1 reaction?
in sn1 reaction the electrophile leaves the substrate forming a carboncation.afterwards the nucleophile while attack the carboncation and usually recimes may be formed in sn1 reaction depending on whether the carboncation experienced a front of backside attack. in sn2 reaction the departing and attacking proccess occurs at the same time. these is pule rampai from the university of johannesburg
What is product adaptation?
Product adaptation is a kind of marketing strategy wherein a company develop new products. The new product is based on modification of existing items.
Why primary alkyl halide are not syntesized using Sn1 reaction?
as order of reactivity of sn1 reaction is 3>2>1 , we do not synthesise primary alkyl halide using sn1 reation. as there is no pushing from other carbon atoms, it is difficult for the X part of RX to separate itself.
What kind of reaction -SN1 or SN2 or E1 or E2- is expected for secondary haloalkanes with sterically hindered strong bases?
the mostly undergo SN1 or E1.. but ratio of E1 is higher...
Aryl halide do not undergo SN reaction?
Do not undergo SN1 reactions.
