How is F-CH2+ a more stable carbocation than (CH3)3C+ though it is the upper limit of hyperconjugation ....Is there back bonding in the first compound .

If yes then how..Plz explain

Can someone help me identify the functional groups in ascorbic acid?

I just started organic chemistry and am having a hard time identifying functional groups.

Calculate the experimental specific rotation (°) of the equilibrium mixture of α- and β-lactose

Calculate the experimental specific rotation (°) of lactose at time equals zero (t = 0)=87 Enter the observed rotation of the equilibrium mixture of α- and β-lactose (°)=5.2 Calculate...

the reactions of amines and it's solubility

How does the solubility in water differ for the nitrogen containing compounds? Suggest reasons for this.What would you expect the solubility in non-aqueous solvents to be? Does your answer to this...

Reactions of amines why butyl amine has a smell

Describe the smell of butyl amine. Can you explain why butyl amine has this smell?

Equations for carboxylic acid

Write an equation for the reaction of ethyl ethanoate with dilute acid, Write a separate equation for the reaction of ethyl ethanoate with dilute alkali. Which one is the preferred...

Reactions of Carboxylic acids

Compare the reactions of ethanoic acid and ethanoyl chloride with ethanol. Explain the differences in their reactions.

Equation for carboxylic acids and their derivatives

Write an equation for the reaction of ethanoic acid with sodium carbonate. How does this reaction compare with that of hydrochloric acid with sodium carbonate?   They look into:  What...

Equation for carboxylic acids and their derivatives

Write an equation for the reaction of PCl5 with ethanoic acid:   and    How might testing pH followed by the reaction with PCl5 be useful in an analysis of an unknown...