Because fluorine has a higher electronegativity
Answer:
Conjugate base: Propionate
Explanation:
- Conjugate base contains one less proton as compared to it's parent acid. Deprotonation occurs from most acidic region.
- Propionic acid deprotonates to produce it's strong conjugate base propionate.
- In propionic acid, -OH group in -COOH functional moiety dissociates to produce
. Because the O-H bond electrons remains highly polarized towards oxygen atom due to electron withdrawing inductive effect as well as resonating effect of -COOH moiety.
- Structure of conjugate base has been shown below.
Answer:Since 1743 the Celsius scale has been based on 0 °C for the freezing point of water and 100 °C for the boiling point of water at 1 atm pressure. Prior to 1743 the values were reversed (i.e. the boiling point was 0 degrees and the freezing point was 100 degrees).
Explanation: i no it
<span>You can compare the strength of the hydrogen bonding by comparing the electronegativities of the other elements. All the four elements, Br, F, Cl and I belong to the same group in the periodic table: group 17 named halogens. Then the kind of bonding they form is similar: polar covalent. You must know the trend of the electronegativities in the periodic table. Electronegativity decrease when you down across a group. Then the electronegativity of F is the higher of the group (indeed, it is the highest of all the 118 elements) . The higher the electronegativity the stronger the attraction that the halogen attracts the electrons and the stronger the hydorgen bonding. Then, the conclusion is that HF has the strongest hydrogen bonding. </span>
Answer:
Alkanes
Explanation:
The description of the first molecule corresponds to a cycloalkane. In the cycloalkanes for each carbon atom there are 2 hydrogen atoms (CnH2n = C5H10).
The second molecule corresponds to an open chain alkane, where for every carbon atom there is double plus 2 hydrogen atoms (CnH (2n + 2) = C5H12)
