The given question is incomplete. The complete question is :
In each row check off the boxes that apply to the underlined reactant. The underlined reactant acts as a... (check all that apply)
1. 
here underlined is 
A. Brønsted-Lowry acid
B. Brønsted-Lowry base
C. Lewis acid
D. Lewis base
2. 
Here underlined is 
A. Brønsted-Lowry acid
B. Brønsted-Lowry base
C. Lewis acid
D. Lewis base
3. 
Here underlined is 
A. Brønsted-Lowry acid
B. Brønsted-Lowry base
C. Lewis acid
D. Lewis base
Answer: 1. Brønsted-Lowry acid
2. Lewis base
3. Brønsted-Lowry base
Explanation:
According to the Bronsted Lowry conjugate acid-base theory, an acid is defined as a substance which donates protons and a base is defined as a substance which accepts protons.
According to the Lewis concept, an acid is defined as a substance that accepts electron pairs and base is defined as a substance which donates electron pairs.
1. 
As 
is donating a proton , it acts as a bronsted acid.
2.
As contains a lone pair of electron on nitrogen , it can easily donate electrons to 
and act as lewi base.
3.
As 
is accepting a proton , it acts as a bronsted base.
Answer:
A concentrated acid is an acid which is in either pure form or has a high concentration. Laboratory type sulfuric acid (about 98% by weight) is a concentrated (and strong) acid. A dilute acid is that in which the concentration of the water mixed in the acid is higher than the concentration of the acid itself.
Explanation:
Concentrated acid - Those acids which are pure or have very high concentration in water are called as concentrated acids. For example concentrated Hydrochloric acid (HCl) and concentrated Sulphuric acid are examples of concentrated acids.
When an atom shares electrons they form a covalent bond.
We need the diagram to answer the question
Answer:
Explanation:
The missing image is attached below.
The objective of this question is to draw the major product formed from the diagram attached below.
From the diagram attached, we will see the reaction of a tertiary alkyl halide together with a weak nucleophile (ch3ch2oh) undergoing a nucleophilic substitution (SN₁) mechanism to yield a racemic mixture(i.e., compound that is not optically active but contains an equal amount of dextrorotatory and levorotatory stereoisomers) as a product.
