Answer:
cyclohexilic acid
Explanation:
The malonic ester synthesis is often used to form different types of carboxilic acid. In this case, we have excess of base, so we can expect a ring formed in the molecule.
In the first step, the base substract the more acidic hydrogen of the ester. In the next step we have the ester reacting with the dibromopentane. Then, in the next step, the excess of base will substract again the acidic hydrogen remaining of the carbon, and then, will promove a Sn2 reaction with the bromine in the pentane (That it was previously attached to the molecule). In this step, a ring id formed. Then, the hydrolisis with acid, will form carboxilic acid in both sides of the molecule, and finally the decarboxilation in heat will separate the molecule and formed the cyclohexilic acid.
The picture below shows the mechanism
Answer:
The equation is already balanced. There's an equal number of materials on each side of the equation.
For metals, reactivity increases down a group and from right to left across a period. Non metals, reactivitt increases up a grouo and from left to right across a period. Francium is the most reactive metal and fluorine is the most reactive non-metal.