The first step in the reaction is the double bond of the Alkene going after the H of HBr. This protonates the Alkene via Markovnikov's rule, and forms a carbocation. The stability of this carbocation dictates the rate of the reaction.
<span>So to solve your problem, protonate all your Alkenes following Markovnikov's rule, and then compare the relative stability of your resulting carbocations. Tertiary is more stable than secondary, so an Alkene that produces a tertiary carbocation reacts faster than an Alkene that produces a secondary carbocation.
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Answer:
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I can't upload further reactions
Explanation:
- sandmeyer's reaction
- swarts reaction
- Finkelstein reaction
- wurtz reaction
- reimer teimann reaction
6. Lucas test
ROH + Zncl2 +HCl ---> RCl + H2O
7. esterification
R-OH +R’-COOH +H+↔ R’-COOR
Answer:
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Answer:Light bounces off of the mirror and then appears to come from behind the mirror.
Explanation:Plane mirrors form images that are virtual, upright and the same size and shape as the object it is reflecting.
When rays of light from the object hits a plane mirror they bounces off the mirror,that is they undergo reflection, and appear to originate from behind the mirror, resulting to the formation of a virtual image.
The image formed appears to be behind the plane in which the mirror lies. A virtual image is an image that is formed at a location from which the rays of light appear to come from. The image can not be formed on a screen..
Answer:
what is the inlet concentration of n-pentane in % by volume? = 34.4%
Explanation:
check below for explanation in the attachment
