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For each of reaction give the expected substitution product and predict whether the mechanism will be first order or second order.

a. 2-chloro-2-methylbutane + CH3COOH
b. Isobutyl bromide + NaOMe
c. 1-iodo-1-methylcylohexane + CH3CH2OH

A certain compound has a solubility of 169 g/L in a solvent. If the mixture contains 50 g of 

solute in a 300 cm3

 of solution, is the solution unsaturated? If yes, how many grams of 

solute should be added to make a saturated solution?


Draw a formula of 3' -uridylic acid, designate types of bonds between the fragments in the molecule. Write schemes of acidic and alkaline hydrolysis of this nucleotide.
a certain compound has a solubility of 169 g/l. of the mixture contains 50 g of solute in 300 cubic cm mixture of solution
A 20.0 g sample of naphthalene, C10H8, is dissolved in 160.7 g of carbon tetrachloride. Calculate the melting point,
boiling point, and osmotic pressure (at 25 ºC) of the resulting solution. (Assume a density of 1.253 g/mL for the
solution).

Draw all of the constitutional isomers that have the formula C5H11F. Circle any structure that is optically active. l. All structures must be drawn as bond-line structures and include any lone pairs of electrons. 


Outline a detailed mechanism for the acid catalyzed hydration of 2 methylbutane with ethanol
Glucose is the most optimal substrate for glycolysis. Polysaccharides amylose, glycogen and cellulose are made of glucose units. Given the premise, these polysaccharides are a better substrates for glycolysis than glucose. Do you agree or not? and why
Give all the possible monohalogenated products of 3-methylpropane +BR2 and indicate major product
Rank the following substances in order of increasing acidity: Acetone, 2,4-Pentanedione, Phenol, Acetic acid
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