Draw the structural formula for both of these alcohols: 2,3, 4-trimethyl, 3-heptanol
4-ethyl, 4-octanol

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explanation:

When naming organic compounds based on IUPAC; we take note of functional group, position of functional group.

In 2,3,4-trimethyl-3-heptanol, the functional group is hydroxyl group ( OH ). It is on position 3 (2,3,4-trimethyl-3-heptanol. Then we put it on the third carbon. Another functional group is methyl group, with three positions, 2, 3, and 4.

In 4-ethyl-4-octanol, the functional group is hydroxyl group ( OH ) which is in position 4 on the fourth carbon. Another functional group is ethyl group in position 4 on the fourth carbon. In this case, the functional groups that have same position, are put on that same carbon.

> b takes place in the gas phase in an isothermal tubular reactor. the feed is one mole of a per one mole of c, an inert. the entering temperature and pressure are 427°c and 10 atm, respectively. the gas constant r = 0.08206 atm · l/mol · k.

the correct answer is b. a strong acid completely dissociates to its ions when dissolved in water. completely dissociates to and ions. a is incorrect because does not fully ionize to and ions and some remain as the compound . c and d are incorrect because, and do not fall into the category of bronsted lowry acids. a bronsted lowry acid is a proton donor and since both molecules do not have a proton to donate they are not bronsted lowry acids. likewise,   if we use the lewis acid definition, they cannot be acids. a lewis acid is an electron pair acceptor. both and have a complete octet so can not accept any electrons which disqualifies them as acids.