Your TA gave you 1 H NMR spectra of your product and iodotyrosine. Using the 1 H NMR spectra and the data given in the special section (p44 and 45), determine the structure of your product - i. E. Do you have ortho-bromo-4-tert-butylphenol, or meta-bromo-4-tert-butylphenol? Explain (using the 1 H NMR) how you came to your decision

yes

Explanation:

given:

mass of na = 115 g

excess cl2

to determine:

mass of nacl produced

explanation:

given reaction is-

2na(s) + cl2(g) → 2nacl(s)

since cl2 is in excess, na will be the limiting reagent

as per the reaction stoichiometry na: nacl = 1: 1

i.e. moles of na reacted = moles of nacl formed

now, # moles of na = mass of na/atomic mass

                                  = 115 g/23 g.mol-1 = 5 moles

therefore, moles of nacl = 5

molar mass of nacl = 58 g/mol

mass of nacl = 5 moles * 58 g.mol-1 = 290 g

ans: amount of nacl produced = 290 g

can you list the answers so i can answer