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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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Answer:
The correct answer to the question is Option E (Strongly retained analytes will give broad peaks).
Explanation:
The other options are true because:
A. Initial temp = 50 °C
Final temp = 270 °C
Differences in temp = 270 - 50 = 220°C
Rate = 10 °C/minute.
So, at 10 °C/minute,
total of 220°C /10 °C = number of minutes required to reach the final temp.
220/10 = 22 minutes
B. A column has a minimum and maximum use temperature. Solutes that are already retained would remain stationary while temperatures are low. This would only change if there is an increase in temperature. Heat transfers more energy to the liquid which would make the solute interact with the column phase.
C. Weakly retained solutes may contain larger molecules, will separate by absorbing into the solvent early in separation making the mobile phase separates out into its components on the stationary phase.
D. Retained solute's vapor pressure is higher at higher temperatures making it possible for particle to escape more from the solute when the temperature is high than when it is low.