The Benzenesulfonic acid does not undergo Friedel-Crafts alkylation because of the deactivation of the compound by the carboxylic group.
<h3>What is the Grignard reagent?</h3>
The Grignard reagent is a compound that contains alkyl magnesium halide.
a) The student will be unsuccessful to prepare a Grignard reagent from 4-bromocyclohexanol because of the -OH group that reacts with the Grignard reagent when formed.
b) The Benzenesulfonic acid does not undergo Friedel-Crafts alkylation because of the deactivation of the compound by the carboxylic group.
c) The compound (2S, 3R)- 2,3-Dibromobutane has a specific rotation, [a]D, 0⁰ because it is a meso compound.
d) This is because, the tertiary alkyl halide is more prone to elimination reaction giving the alkene.
e) This is because, the reaction may be occurring by an SN1 mechanism and the rate determining step is the formation of the carbocation.
Learn more about substitution reaction:brainly.com/question/16811879
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Ok so all are in the alkali family also they are all metals and in group 1 but I think the one that might reacts quickest is Li because it has less AMU
Ummmmmmmmmmmmmmmmmmmmmmmmm, 21
- Glucose = C₆H₁₂O₆.
- Atomic mass of C = 12 u
- Atomic mass of H = 1 u
- Atomic mass of O = 16 u
- Therefore, the molecular mass of glucose
- = (6 × Atomic mass of C) + (12 × Atomic mass of H) + (6 × Atomic mass of O)
- = (6 × 12) + (12 × 1) + (6 × 16) u
- = 72 + 12 + 96 u
- = 180 u
<u>Answer</u><u>:</u>
<u>1</u><u>8</u><u>0</u><u> </u><u>u</u>
Hope you could understand.
If you have any query, feel free to ask.
