Recently Active Organic Chemistry Questions

I KEPt THE NAME OF THE QUESTION AS SUCH BECAUSE I WILL KEEP ON POSTING MY QUESTIONS IN THIS TAG ONLYYYYYYYY I WILL ADD NEW QUESTIONS DAILYYYYYYYYYYYY whats more than organic in chemistry.. so i will start with that 1]Convert ...

Can someone help me why the following compounds do not show tautomerism. *Image* ...

which one is more stable? *Image* ...

Number of unhybridised orbitals in vinyl acetylene are (A) 2 (B) 3 (C) 4 (D) 6 ...

wat is phenoxide moiety?????? ...

hello!! i am nearly a starter in ORGANIC CHEMISTRY!! i am presently using a book ORGANIC CHEMISTRY ARIHANT PUBLICATIONS... Is this book good enough??I mean which is the best book to use to gain best and clearest theoritical c ...

The smallest ketone and its next homologue are reacted with NH2OH to forn oxime. (a) two different oximes are formed. (b)three diff oximes are formed . (c)two oximes are optically active. (d) all oximes are optically active. ...

well....organic a nightmare for many fun for others....a house of many exceptions to basic phenomenon n reactions is the beauty of ORGANIC CHEMISTRY!!!!!!! so this thread is dedicated to those exceptions in organic chemistry! ...

*Image* I THINK WE WILL GET *Image* AM I CORRECT??????????????? ...

does tolllens reagent oxidize alcohols and giv a positive test for thm too wat bout fehlings and benedicts? ...

The IUPAC name of [CuCl2{O=C(NH2)2}2] is A) dichloridobis(urea)copper(II) B) bis(urea)dichloridocopper(II) C) dichloridobis(ureaido)copper(II) D) bis(ureaido)dichloridocopper(II) ...

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What is disiamyl borane and DBN? ...

whats the mechanism?? *Image* ...

what is the mechanism for the intramolecular wurtz reaction? ...

What explains the fact that methanol reacts with HX faster than a primary alcohol? ...

Why is pyridine used in the reaction of R-OH + PCl3 to make R-Cl? ...

Whats products we obtain when ethyl propanoate reacts with C6H5MgBr then H2O + NH4Cl? Please so the mechanism ...

In the following compounds, *Image* The order of basicity is a) IV > I > III> II b) III > I > IV > II c) II > I > III > IV d) I > III > II > IV ...

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Why is cyclopropane forming from an alkene in Simmons Smith reaction? Isn't dat increasing d strain...i mean isn't d product more unstable dan d reactant???? Heres wat i got for d reaction mechanism... *Image* ...

What is the mechanism of the reaction- Na+C- *Image* C-Na++2CO2→Na+O-OCC *Image* CCOO-Na+ ...

3)Which of the following statement is wrong? a the IUPAC name of alkenes ends with suffix –ene b the IUPAC name of alkynes ends with suffix –yne c the substituents gets lower number in comparison to functional group d the ...

My first question is how bond angle is related to pKa values of a compound....Heres d question Q1. Selected bond angles for five hydrocarbons are shown below. Arrange these hydrocarbons according to their pKa values, from low ...

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*Image* The answer is B......ok dats fine dat a cabocation will form so it prooceeds in forward direction....but wouldn't d C option should also be correct......Why we r not accounting for d resonance stabilisation of RCOO-?? ...

What is the difference between regiospecific and regioselective; and stereospecific and stereoselective? ...

Why are beta keto acids unstable? Or the other way round....Why do beta keto acids undergo decarboxylation easily? Can't just find a good reason for this..... ...

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