Based on the theoretical result, what is the order of reactivity of primary, secondary, and tertiary alkyl halides with sodium iodide in acetone? Based on the theoretical result, what is the order of reactivity of primary, secondary, and tertiary alkyl halides with ethanolic silver nitrate? In the Silver Nitrate Test, which is more reactive benzyl chloride or chlorobenzene? Compare SN1 and SN2 Reactions of Alkyl Halides

In mass spectrometry, McLafferty Rearrangements are common in carbonyl compounds. Draw the daughter ion that would be observed in the mass spectrum resulting from McLafferty Rearragments of this molecule.

What is the energy diagram of the following Sn1 reaction.   2-chloro-2-methylpropane + H2O -> 2-methylpropan-2-ol + HCl   write the rate law equation

The sodium iodide test is used to identify primary alkyl halides and it also takes place via a substitution reaction.Describe the test including the reactions that explain the full mechanism. Explain whether this reaction follows aSN1 or a SN2 mechanism.

Ethers can often be prepared by SN2 reaction of alkoxide ions, RO*, with alkyl halides. Which of the two possible routes would be the better choice to synthesize the molecule shown below? Explain briefly.

An organic chemistry experiment involves a nucleophilic substitution (SN2) reaction using 1-iodobutane and 2-naphthoxide ion. The 2-naphthoxide ion is generated from 2-naphthol and sodium hydroxide in an ethanol solvent. The experiment includes steps like generating the nucleophile, conducting the SN2 reaction, and analyzing the product using 1H NMR spectroscopy. Question: On the 1H NMR spectra (attached), draw the structure of the product and assign the peaks. Label the unique protons with different letters and write those same letters by the peaks in the NMR spectrum.

How does increasing base, solvent, or alkyl halide or aptly halide + base affect or decreasing them affect the reaction rate for e2/e1 and sn2/sn1? Please provide examples

Imagine that phenol (“hydroxybenzene”) and nitrobenzene are reacted (in separate beakers) with a hot solution containing both concentrated sulfuric acid and concentrated nitric acid. A) Phenol reacts much more quickly than benzene, and benzene reacts much more quickly that nitrobenzene. Explain this observation, using at least one appropriate reaction coordinate diagram as part of your answer (be sure to label your reaction diagram with appropriate structures). You do not need to include any complete mechanisms, but you may wish to use portions of mechanisms as part of your discussion.