How to use both 1H and 13C NMR spectroscopy to tell difference between isomeric COOH's

Indicate how you would use both 1H and 13C NMR spectroscopy to tell the difference between these isomeric carboxylic acids: succinic acid - HO2CCH2CH2COOH methylmalonic acid - CH3CH(COOH)2

Which carboxyl group is more acidic in 3-chlorohexanedioic acid?

The 2 carboxyl groups in 3-chlorohexanedioic acid are not equivalent and have different dissociation constants. Which carboxylic group is more acidic? Please explain.

Equation showing salt formation from adipic acid + ethyl amine

Write an equation that shows the formation of salt that can be formed by reaction of 1mol of adipic acid + 2 mol of ethylamine.

orgainc reactions

Reaction 1 Reaction 2 O // CH3--C==CH--CH2--OH + CH3--CH2--C ! CH3 OH ? Reaction 1 between compounds 1 and 2. The equation is incomplete only the reactants are shown, the missing product(s) where ? is. What is the product(s) Identify the functional groups in reaction 1 and 2. Complete the equation for reaction 1 by drawing the abbreviated structual formula of the product in place of the question mark and then identify any new functional group in the organic products. I have done this question but would like to know if... click for more

draw abbr. structural formulae

Draw abbrivated structural formulae of the prouducts of the complete hydrolysis of lidocaine. identity the functional groups. 1st Diagram Lidocaine is thought to bind to receptors in its methylated form. Identify in writing the atoms or groups that could be involved in its binding to a receptor via hydrogen bonding (only 1 example) and ionic reaction 2nd diagram Give examples of the types of functional group that need to be present in the receptor sites in order for these forms of binding to take place (1 example from each binding) I have my answers to this I would like to know if I am on the right track Thanks