Answer:
a) The structure of anthracene is planar with all the pi electrons delocalized in the structure to maintain aromaticity.
b) The C-C bond length in anthracene is about 140 pm with all the bond lengths being similar to each other.
The standard C-C bond length is 154 pm while standard C=C bond is about 134 pm. Therefore the bond length in anthracene is smaller than standard C-C bond length and longer than standard C=C bond length. This can be explained from the fact that the C-C bonds in anthracene has be mixed characteristics of single and double bond because of the delocalization of pi electrons over the whole structure. As a result, they are neither fully single nor fully double bond in nature. Hence the observed bond lengths.
c) This molecule is not flat. The N-atom is sp3 hybridized here and the H-atom attached to N will remain out of plane.
Explanation:
Answer:
The answer to your question is below
Explanation:
There are two kinds of mixtures
- Homogeneous is a mixture of two or more elements or compounds and its components can not be distinguished visually.
- Heterogeneous is a mixture of two or more elements or compounds and its components can be distinguished visually.
a cup of tea and sugar homogeneous
peanuts and almonds mixed together in a bowl heterogeneous
a bucket full of sand and gravel heterogeneous
food coloring dissolved in water homogeneous
Answer:
The answer is (A)
Explanation:
When the weather changes, nature also changes because most plants rely on photosynthesis and if they don't get as much light then they can't support as much as they used causing them to shut down parts of the plant.
The whole Activity , poem and paragraph is missing in the question.
Answer:
(1) Liquid A
(2) Solid A
Explanation:
Using this part of the given poem
Substances and mixtures behave differently,
During boiling and melting most especially
Boiling point of substance is fixed while mixture is not
Substance melts completely but mixture does not
The boiling point of the Pure substance remain fixed after reaching its boiling point this is shown by Liquid A
Solid A is melting completely so Solid A is a pure substance.
Answer:
a. electrophilic aromatic substitution
b. nucleophilic aromatic substitution
c. nucleophilic aromatic substitution
d. electrophilic aromatic substitution
e. nucleophilic aromatic substitution
f. electrophilic aromatic substitution
Explanation:
Electrophilic aromatic substitution is a type of chemical reaction where a hydrogen atom or a functional group that is attached to the aromatic ring is replaced by an electrophile. Electrophilic aromatic substitutions can be classified into five classes: 1-Halogenation: is the replacement of one or more hydrogen (H) atoms in an organic compound by a halogen such as, for example, bromine (bromination), chlorine (chlorination), etc; 2- Nitration: the replacement of H with a nitrate group (NO2); 3-Sulfonation: the replacement of H with a bisulfite (SO3H); 4-Friedel-CraftsAlkylation: the replacement of H with an alkyl group (R), and 5-Friedel-Crafts Acylation: the replacement of H with an acyl group (RCO). For example, the Benzene undergoes electrophilic substitution to produce a wide range of chemical compounds (chlorobenzene, nitrobenzene, benzene sulfonic acid, etc).
A nucleophilic aromatic substitution is a type of chemical reaction where an electron-rich nucleophile displaces a leaving group (for example, a halide on the aromatic ring). There are six types of nucleophilic substitution mechanisms: 1-the SNAr (addition-elimination) mechanism, whose name is due to the Hughes-Ingold symbol ''SN' and a unimolecular mechanism; 2-the SN1 reaction that produces diazonium salts 3-the benzyne mechanism that produce highly reactive species (including benzyne) derived from the aromatic ring by the replacement of two substituents; 4-the free radical SRN1 mechanism where a substituent on the aromatic ring is displaced by a nucleophile with the formation of intermediary free radical species; 5-the ANRORC (Addition of the Nucleophile, Ring Opening, and Ring Closure) mechanism, involved in reactions of metal amide nucleophiles and substituted pyrimidines; and 6-the Vicarious nucleophilic substitution, where a nucleophile displaces an H atom on the aromatic ring but without leaving groups (such as, for example, halogen substituents).