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What else can I help you with?
Is triphenylmethanol soluble in chloroform?
Yes, triphenylmethanol is soluble in chloroform. This is because both triphenylmethanol and chloroform are nonpolar molecules, which allows them to dissolve in each other.
What is the mechanism for the reaction of triphenylmethanol with HBr?
In the reaction of triphenylmethanol with HBr, the acidic proton of HBr protonates the hydroxyl group of triphenylmethanol to form water and triphenylmethyl cation. This triphenylmethyl cation then undergoes bromide ion attack to form triphenylmethyl bromide.
Why must the reaction for the synthesis of triphenylmethanol be anhydrous?
The reaction for the synthesis of triphenylmethanol must be anhydrous because water can react with the reagents and interfere with the desired chemical reaction, leading to lower yields or undesired byproducts. Anhydrous conditions help ensure the reaction proceeds smoothly and efficiently.
Interpret the principal peaks in the infrared spectrm of either triphenylmethanol?
The infrared spectrum of triphenylmethanol will have a broad peak for the OH group at 3550 - 3200 cm^-1. It will also have a C-O peak at 1300 - 1000 cm^-1. Because of the aromatic C=C groups in the three benzene rings, there will be prominent peaks around 1600 - 1585 cm ^-1 and 1500 - 1400 cm^-1.
Is triphenylmethanol polar or non polar?
Triphenylmethanol is considered polar due to the presence of a hydroxyl (OH) group, which creates an uneven distribution of electron density in the molecule. This results in a slightly negative charge near the oxygen atom and a slightly positive charge on the phenyl rings, leading to overall polarity in the compound.
What is the chemical formula of triphenylmethanol?
The chemical formula of triphenylmethanol is C19H16O.
Is triphenylmethanol soluble in chloroform?
Yes, triphenylmethanol is soluble in chloroform. This is because both triphenylmethanol and chloroform are nonpolar molecules, which allows them to dissolve in each other.
Ir of triphenylmethanol?
NO
What is the mechanism for the reaction of triphenylmethanol with HBr?
In the reaction of triphenylmethanol with HBr, the acidic proton of HBr protonates the hydroxyl group of triphenylmethanol to form water and triphenylmethyl cation. This triphenylmethyl cation then undergoes bromide ion attack to form triphenylmethyl bromide.
Why must the reaction for the synthesis of triphenylmethanol be anhydrous?
The reaction for the synthesis of triphenylmethanol must be anhydrous because water can react with the reagents and interfere with the desired chemical reaction, leading to lower yields or undesired byproducts. Anhydrous conditions help ensure the reaction proceeds smoothly and efficiently.
If ethyl benzoate used to prepare triphenylmethanol is wet what byproduct is formed?
THIS IS A DIRECT QUOTE FROM YAHOO ANSWERS:Benzene and magnesium hydroxide and magnesium bromide.I am betting you are doing a Grignard reactionEthyl benzoate + 2 phenylmagnesium bromide --> triphenylmethanol•MgBr saltif water is present, the grignard reacts with the water firstPhenylmagnesium bromide + H2O --> benzene + MgOHBr
Interpret the principal peaks in the infrared spectrm of either triphenylmethanol?
The infrared spectrum of triphenylmethanol will have a broad peak for the OH group at 3550 - 3200 cm^-1. It will also have a C-O peak at 1300 - 1000 cm^-1. Because of the aromatic C=C groups in the three benzene rings, there will be prominent peaks around 1600 - 1585 cm ^-1 and 1500 - 1400 cm^-1.
Is triphenylmethanol polar or non polar?
Triphenylmethanol is considered polar due to the presence of a hydroxyl (OH) group, which creates an uneven distribution of electron density in the molecule. This results in a slightly negative charge near the oxygen atom and a slightly positive charge on the phenyl rings, leading to overall polarity in the compound.
If ethyl benzoate is treated with phenylmagnesium bromide a one to one mixture of benzophenone and triphenylmethanol are obtained after work-up. Why?
The MgBr causes the carbon that it's attached to in the phenylmagnesium bromide to become negative and attack the carbonyl carbon of the ethyl benzoate. The carbonly obtains a new bond with a phenyl group and loses its double bond to oxygen. It instead becomes a single bond and oxygen becomes negative (theoretically, the MgBr will attach to the oxygen as an intermediate phase). This attack of the carbon attached to the MgBr will happen a second time creating a carbon attached to 3 phenyl groups (triphenyl) and upon reduction of this compound (using H2 and a catalyst or LiAlH4), -OCH2CH3 gets protonated and leaves as ethanol, and the carbon and oxygen get protonated to CH3OH. I hope this makes sense to you, lol.
How did Livingstone decide to go to Africa?
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What is the job market for acting?
yes acting is hard, if we are talking about the good acting (well yes its hard), but if we are talking about the sloopy acting of course its easy. for acting you have to have a lot of concentration and you have to know a lot of basic things that most of the people that take classes of acting and that they are professional actors do bnot know. some of you people wont know what blocking a scene is, or maybe you guys dont know that you have to mantaing a balance on scene, also you have to know about diction and other stuff to, acting is not all about you learn your lines you do your part good and evreybody gives you a round of applusse. no an actor is much more thatn that. i know cause i am an actor and most of the people that i know that call themselves actor do not know some of thoose basic stuff.
What is the color of absence of color?
The color of absence of color is white.
