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the solvolysis of 2-bromo-3-methylbutane potentially can give several products, including both e1 and s n 1 products from both the unrearranged carbocation and the rearranged carbocation. part b indicate whether the products are from e1 or s n 1 reactions. drag the appropriate products to their respective bins.

Respuesta :

SN1 interactions with allylic electrophiles, lamp fuel, and valuable component in skincare and cosmetics products.

What purposes do E1 reactions serve?

It is common practice to convert saturated compounds (organic molecules with single carbon-carbon bonds) into unsaturated compounds using an elimination reaction (compounds which feature double or triple carbon-carbon bonds).

What circumstances are favorable for SN1 and E1 reactions?

The required carbocation intermediate must typically be somewhat stable for an SN1 or E1 reaction to take place. Strong bases, particularly strong hindered bases (such tert-butoxide), promote elimination while strong nucleophiles, especially strong, favor replacement. Small groups on the carbon attached to halogen atom.

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