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Ira Lisetskai [31]
3 years ago
6

Please help me school ends tomorrow

Chemistry
1 answer:
wolverine [178]3 years ago
3 0

Answer:

<h2>D) clapping hands </h2>

Explanation:

hope it's helpful

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What is the answer?? I need help
professor190 [17]

Answer:

covalent

Explanation:

flourine and sulfur are both nonmetals/anions, therefore it is covalent.

6 0
3 years ago
What Is Modern Methods Of Agriculture Practices And its Advantages?
Olin [163]

Answer:

Explanation:

Modern Agriculture - The agricultural practices with modern technique like Fertilizers, Innovative hybrid seed, and utilization of machine call modern Agriculture.

Advantages -

Feeding to the population without scarcity of food grains.

Optimum Utilization of land (Crop intensity more then 300%)

Increased production of food grain.

Global Market - even our mangoes available at US and we are getting California apple too.

Due to factories and Machine use this industry is growing to and empowering good employment.

I hope this helps you :)

7 0
4 years ago
Why do the carbon anodes need to be replaced regularly in the electrolysis of Al2O3 into aluminum metal?
Nuetrik [128]

Answer:

A) They get oxidized into carbon monoxide and carbon dioxide by the oxygen molecules generated on the electrode.

Explanation:

In the electrolysis of Aluminium, the oxygen reacts with the carbon anodes forming carbon dioxide. That is, the anodes are oxidized. To ensure that the reaction completes, the anode must gradually be replaced as the reaction proceeds. The correct option is hence;

A) They get oxidized into carbon monoxide and carbon dioxide by the oxygen molecules generated on the electrode.

8 0
3 years ago
How are sound waves different from the waves in the sea or the ripples on water???
nirvana33 [79]

Answer:

water wave shake energy over the surface to the sea, while sound waves thump energy trough the body of the air. sound waves are compression waves

<em>Hope</em><em> this</em><em> </em><em>helps</em><em> </em><em>:</em><em>)</em>

5 0
3 years ago
Determine whether each description applies to electrophilic aromatic substitution or nucleophilic aromatic substitution.
Alborosie

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).

3 0
3 years ago
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