1. why is toluene a stronger nucleophile than benzene?
2.why is phenol a stronger nucleophile than benzene?
1. In Toluene, The -CH3 group attached to benzene is a mild activating group. It
does not make benzene more reactive but only slightly so. methyl group activates the benzene ring towards electrophiles.
2. In Phenols, The -OH group attached to benzene is a highly activating group. The lone pair on oxygen is delocalised into the benzene ring and makes benzene very electron rich. this makes benzene very attractive towards electrophiles. so reaction with electrophilic reagents occur at milder conditions.
In both of the conditions, benzene ring activated by the -CH3 and -OH group and increases the nucleophilic nature of the benzene ring. So that the toluene and phenol is stronger nucleophile than benzene. between toluene and phenol, phenol is stronger nucleophile than toluene.
i hope you will understand well.....thank you ?
1. why is toluene a stronger nucleophile than benzene? 2.why is phenol a stronger nucleophile than...
1. why is toluene a stronger nucleophile than benzene? 2.why is phenol a stronger nucleophile than benzene?
Which of the choices explains why one nucleophile is stronger than another nucleophile? More than one answer is possible. It is also possible that NONE of these is correct. 7 A stronger nucleophile is larger than another nucleophile. A stronger nucleophile has a less electronegative nucleophilic atom than another nucleophile. A stronger nucleophile has less steric hindrance than another nucleophile. Using this information, in methanol, CH3OH, which of the following is a stronger nucleophile, trimethylamine, (CH3)3N, or dimethylether, (CH3)20? SS...
Propose syntheses of the following molecules, starting from
benzene, toluene or phenol, any inorganic reagents and any organic
reagent of TWO carbons or less:
4. Propose syntheses of the following molecules, starting from benzene, toluene or phenol, any inorganic reagents and any organi c reagent of TWO carbons or le a) NO2 b) CO2H c) OH d) e) NO2 NO2 Br CI CI CO2H Br
1.In the following chromatogram, a mixture of pyridine (1),
phenol (2), and toluene (3) was separated. Determine the retention
times of the components. Given this order of elution, would you
expect the stationary phase to be polar or non-polar?
Explain why the toluene peak is much shorter than the other two
peaks even though it is approximately the same concentration.
2. Stationary phases come in different varieties. Which of the
two analytes listed for each stationary phase has the greater...
1. Why is there an ease of nitration and bromination of phenol relative to benzene? 2. What are some reactions of alcohols: - oxidation, dehydration, esterification, acylation.
Show how you would synthesize each compound from benzene, toluene, or phenol using the following reactions: Reactions 1. Halogenation 2. Nitration 3. Sulfonation 4. Friedel-Crafts acylation 5. Friedel-Crafts alkylation 6. Oxidation of methyl group 7. Reduction of nitro group • Choose the starting material from the drop-down list • Enter the number(s) of the desired reactions in the order that you wish to use them without commas between • If a reaction is used more than once, enter its number...
Free Radical Bromination: The four aromatic hydrocarbons, toluene, ethyl-benzene, isopropyl benzene, and t-butyl benzene is treated with Br2 in CH2Cl2. The solution reacted in this order (first to last): isopropyl benzene, ethyl-benzene, toluene, and t-butyl benzene. Can someone please explain why this order of reaction happened? in relation to their structure?
7% Xylene 4% Styrene 54% Toluene 35% Benzene 18% Xylene 24% Styrene 42%Toluene 16% Benzene { 15% Xylene 25% Styrene 40% Toluene 20% Benzene 15% Xylene 10% Styrene 54% Toluene 21% Benzene D F- 24% Xylene 65% Styrene 10% Toluene 1% Benzene 105 kg/min Xylene 0.07 0.18 0.15 0.24 внS Xylene INV 281048 1.221774 1A0342 6.0004 175 kg/mn 28 kg/min 14 kg/min Styrene 0.04 0.24 0.65 Styrene 94.3629 -25.83c6 -35.6855 41.1371 Teluene 0.54 0.42 0.54 0.1 Toluene -66.0444 20.24557 30.52823...
1. Why is it important to mix the phenol with sodium hydroxide before adding the chlorobutane? What happens during this time? 2. Why does phenol react with sodium hydroxide? Why does ethanol not react to the extent that phenol does with sodium hydroxide? 3. What is the better nucleophile, sodium phenoxide or phenol? Why? 4. Why do you need to rinse your product with ice water instead of room temperature water?
Consider the reactivity of phenol, bromobenzene, toluene, and nitrobenzene toward electrophilic aromatic substitution. 1.) The most reactive compound is (pick one: phenol, bromobenzene, toluene, and nitrobenzene) because the (pick one: electron donating or electron withdrawing) character of the (pick one: alcohol group, methyl group, bromine atom, or nitro group) increases the rate of the reaction. 2.) The least reactive compound is (pick one: phenol, bromobenzene, toluene, and nitrobenzene) because the (pick one: electron donating or electron withdrawing) character of the...