Choose any bases that will selectively deprotonate the above acid, that is, any bases that will favor the formation of products.
Choose Any Bases That Will Selectively Deprotonate The Above Acid, That Is, Any Bases That Will Favor The Formation Of Products.
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Choose Any Bases That Will Selectively Deprotonate The Above Acid, That Is, Any Bases That Will Favor The Formation Of Products.. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below. Your solution’s ready to go!
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To deprotonate a molecule effectively, it's crucial to select a base that is sufficiently strong for the task while avoiding bases that are too aggressive to handle safely. So, a base can deprotonate an acid if the conjugate acid of the base has a higher pk a than the given acid. See examples of deprotonating phenol, alkyne,.
To Deprotonate A Molecule Effectively, It's Crucial To Select A Base That Is Sufficiently Strong For The Task While Avoiding Bases That Are Too Aggressive To Handle Safely.
Based on the given options, nah and nanh2 are strong bases that can selectively deprotonate the acid. Your solution’s ready to go! An acid must have a higher pk a to deprotonate another acid.
Learn The Principle Of Choosing A Base To Deprotonate A Given Compound Based On The Pka Values Of Acids And Bases.
See examples of deprotonating phenol, alkyne,. Nah o nanh2 nh3 nahco3 phona naoh. Solution for choose any bases that will selectively deprotonate the.
So, A Base Can Deprotonate An Acid If The Conjugate Acid Of The Base Has A Higher Pk A Than The Given Acid.
Learn more about this topic, chemistry and related others by exploring similar questions and additional content below. To selectively deprotonate cyclohexanol and favor the formation of products, we should choose strong bases that can abstract the acidic hydrogen.