You can start with 2- propanol, react it with sodium so that you get the alkoxide ion of the two reactant then follow it with an alkylhalide so that a nucleophilic substitution reaction can take place to form 2-methoxypropane. An alkylhalide to be used here be an alkyl of any of the halogen group or aklylsulfonate/aklylsulfate can be used also instead of alkylhalide
in first step prepare ethane to chloro ethane fallowed by wurtz reaction. chloro ethane can be prepared free radical reaction btw ethane and chlorine
When you attempt to prepare sulfanilamide from this reagent, a polymeric product is produced after the addition of PCL5 in step one. So no, this is not typically a reaction used to prepare sulfanilamide.
CaOCl2+ H2O=Ca(OH)2+Cl2
dehydration
The reaction is possible in the presence of sodium dichromate and sulfuric acid.
Photosynthetic organisms "prepare" food by synthesis from light thus Photo-synthesis.. synthesis means to make, to produce.
We can prepare KCN by the reaction of KOH and HCN.Where HCN can be generated by the pyrolysis of formamide.
prepare citric acid using reformatsky reaction
in first step prepare ethane to chloro ethane fallowed by wurtz reaction. chloro ethane can be prepared free radical reaction btw ethane and chlorine
he gave an encouriging speech
this process is called photosynthesis (photo-light, synthesis-to prepare).
Precipitation
KOH is used to prepare liquid soaps.
The asymmetric Strecker synthesis is a method used to prepare chiral α-amino nitriles from aldehydes and primary amines. In the case of clopidogrel, the synthesis involves the formation of the chiral α-amino nitrile, which is subsequently converted into the desired thienopyridine structure through further chemical reactions. The final steps in the synthesis involve the introduction of the clopidogrel-specific moieties to complete the synthesis of clopidogrel.
Answer He had them ready for William to attack
he prepeare by washing his face and hands
When you attempt to prepare sulfanilamide from this reagent, a polymeric product is produced after the addition of PCL5 in step one. So no, this is not typically a reaction used to prepare sulfanilamide.