[cs_content][cs_section parallax=”false” separator_top_type=”none” separator_top_height=”50px” separator_top_angle_point=”50″ separator_bottom_type=”none” separator_bottom_height=”50px” separator_bottom_angle_point=”50″ style=”margin: 0px;padding: 45px 0px;”][cs_row inner_container=”true” marginless_columns=”false” style=”margin: 0px auto;padding: 0px;”][cs_column fade=”false” fade_animation=”in” fade_animation_offset=”45px” fade_duration=”750″ type=”1/1″ style=”padding: 0px;”][cs_text]The Acidic Environment > 5. Esterification >
Explain the difference in melting point and boiling point caused by straight-chained alkanoic acid and straight-chained primary alkanol structures[/cs_text][/cs_column][/cs_row][/cs_section][cs_section parallax=”false” separator_top_type=”none” separator_top_height=”50px” separator_top_angle_point=”50″ separator_bottom_type=”none” separator_bottom_height=”50px” separator_bottom_angle_point=”50″ style=”margin: 0px;padding: 45px 0px;”][cs_row inner_container=”true” marginless_columns=”false” style=”margin: 0px auto;padding: 0px;”][cs_column fade=”false” fade_animation=”in” fade_animation_offset=”45px” fade_duration=”750″ type=”1/1″ style=”padding: 0px;”][cs_text]
- Hydrogen bonding occurs between alkanols (a bond between a hydrogen atom of one molecule and an oxygen atom of a nearby molecule), causing them to have higher melting and boiling points than alkanes of similar molar mass.
- A greater amount of hydrogen bonding occurs between alkanoic acids (two bonds between a hydrogen and an oxygen atom of one molecule and a hydrogen and an oxygen atom of a nearby molecule), causing them to have even higher melting and boiling points than alkanols of the same molar mass.
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