Question

Draw the condensed structural formulas for $a$and $b$and lineangle formulas for $c$and $d$:

a. hexyl acetate

b. ethyl methanoate

c. propyl benzoate

d. methyl octanoate

Short answer

(part a)

(part b)

(part c)

(part d)

Step-by-step solution

Introduction  (part  a)

Carboxylic acids are weak acids that reduce basic by releasing hydrogen ion salts. The carboxyl group of either a carbocation is bonded to either a phenyl ring to produce a methyl group with carbonyl group. An methyl or benzyl component may engage to the carboxyl member.

Given Information (part a) 

When strong acids combine with strong acids including $-OH$and $-H$ to create carboxy compounds, these become entirely negated. By exchanging the ic acid (at the end) and ended up eating, the acetate cation is termed.

Explanation (part a)

(a) Hexyl acetate compacted balanced equation was

Given Information (part b)

When strong acids combine with strong acids including $-OH$and $-H$ to create carboxy compounds, these become entirely negated. By exchanging the ic acid (at the end) and ended up eating, the acetate cation is termed.

Explanation (part b)

(b) Ethyl methanoate compacted balanced equation was

Given Information (part c)

When strong acids combine with strong acids including $-OH$and$-H$ to create carboxy compounds, these become entirely negated. By exchanging the ic acid (at the end) and ended up eating, the acetate cation is termed.

Explanation (part c)

(c) The formula for propyl benzoate line-angle equation becomes

Given Information (part d)

When strong acids combine with strong acids including $-OH$and $-H$ to create carboxy compounds, these become entirely negated. By exchanging the ic acid (at the end) and ended up eating, the acetate cation is termed.

Explanation (part d)

(d) The formula for methyl octanoate line-angle equation becomes