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you react the grignard with either an ester, an acid chloride or a ketone to get a tertiary alchohol. if you react a grignard reagent with an aldehyde you get a secondary alcohol and if you react the grignard with formaldehyde (methenal) you get a primary alchohol. same thing happens if u use R-Li instead of a grignard reagant.
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How do you make dimethyl titanocene?
Titanocene dichloride &methyl grignard in toluene medium at 5'c
Does the excess reagent determine the amount of a product?
The limiting reagent is the determinant because you can only make as much as the smallest amount can provide to react with
What tertiary colors make the color plum?
Red and blue
What is foulger's reagent?
40g urea+ 80ml of 40%H2SO4! add 2g stannous chloride, heat untill solution is clear and make the volume upto 100ml. it is called foulger's reagent!
How do you prepare toluene reagent from benzen?
treat benzene with CO/CuCl/AlCl3/HCl to make a benzaldehyde (i.e. add CHO on benzene ring), then Zn(Hg)/HCl to make toluene
Why grignard reagent always kept in dry ether?
During the formation of Grignard's reagent dry or anhydrous ether is used to prevent the magnesium from moisture because in presence of water magnesium leaves the organic material and combines with water.
What is the equation for the preparation of ketones from secondary alcohols?
You can only make any ketone from any secondary alcohol by using PCC, Jones reagent, or NaCr2O4 in acid as a reagent.
What will you do if you transfer a reagent to another reagent?
i dont quite understand what your saying but if you mean using reagents to make a reagent like transmute bone. when you make the bone or whatever you will get rid of about 2 reagents to make one hard to find reagent to me not worth it. -Zarchary DayGlen on wizard101
How do you make dimethyl titanocene?
Titanocene dichloride &methyl grignard in toluene medium at 5'c
How do you detect benzene in the Grignard synthesis of benzoic acid?
Not sure what you mean... If you mean 'how is benzene used for the Grignard synthesis of Benzoic Acid,' then the answer is, bromobenzene (C6H5Br) is turned into phenyl Grignard (C6H5MgBr) by the addition of Magnesium in ether, and then dry ice (solid CO2) is added to the reaction mixture to make Benzoate (C6H5COO-), which is the conjugate base of Benzoic Acid. That has got to help you somehow.
Does the excess reagent determine the amount of a product?
The limiting reagent is the determinant because you can only make as much as the smallest amount can provide to react with
What makes Alton towers the tertiary sector?
Entertainment and Tourism are the key areas that make the Tertiary sector
Is an alcohol better leaving group than cyano group?
Although cyano isn't a very good leaving group (it IS a fantastic nucleophile, however), it is still better than an alcohol. The only way you can make an alcohol a good leaving group is to activate it somehow. Methods range from simple protonation (making [H-OH]+ - water) in an acidic environment, to tosyl-/mesylation to make OTs/OMs, to activation with a phosphorous reagent, etc.
What does a primary color and secondary color make?
A tertiary colour.
What tertiary colors make the color plum?
Red and blue
What does the seconardy tertiary industries do?
Secondary and tertiary industries make parts or sub-assemblies, or provide specialized services or personnel, for the main manufacturers.
What is foulger's reagent?
40g urea+ 80ml of 40%H2SO4! add 2g stannous chloride, heat untill solution is clear and make the volume upto 100ml. it is called foulger's reagent!
