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vesna_86 [32]
3 years ago
11

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Chemistry
1 answer:
Bogdan [553]3 years ago
5 0

Answer:

katniss and peeta love each toher

Explanation:

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Help me 20 points please someone just get this done
faust18 [17]

Answer:

whut done

Explanation:

I ain't see nothing

6 0
3 years ago
Read 2 more answers
Which feature causes a gap in the geologic record?
Serhud [2]

Answer:

Hi, there the answer is

A)extrusion

Explanation:

5 0
3 years ago
If an object has 25 newtons of force pushing from the left and 26 newtons of force pushing from the right the object will
IRISSAK [1]

Answer:

C. move left

Explanation:

The object will move towards the left direction due to the unbalanced forces that are acting on it.

 The resultant force on the object will be 1N in the left direction

  • The resultant force on a body is that singular force that will have the same effect as the different forces that acts on a body
  • When forces acts in opposite directions, they are subtracted
  • The object will move in the direction of the one with the greater force

So;

  Resultant force = 26N - 25N  = 1N

The body moves 1N to the left

7 0
2 years ago
What can be used to determine the absolute age of two rocks? *
Aneli [31]

Answer:Ithink erosion cuz if we can tell how long ago it eroded we can see how old it is

Explanation:

6 0
2 years ago
Name a possible product of this reaction in the presence of ether and AlCl3: methylbenzene + 1-chlorodecane.a. 1-methyl-2-decylb
Vikki [24]

Answer:

None of these

Explanation:

Friedel–Craft reaction is a reaction involves the attachment of substituents to the benzene ring.

Mechanism of the reaction of methylbenzene with 1-chlorodecane in the presence of ether and aluminum chloride :

Step -1 : Generation of stable carbocation.

Aluminium chloride acts as Lewis acid which removes the chloride ion from the alkyl halide forming carbocation. The primary carbocation thus formed gets rearranged to secondary primary carbocation which is more stable due to hyperconjugation.

Step-2: Attack of the ring to the carbocation

The pi electrons of the ring behave as a nucleophile and attacks the carbocation. Since, the group attached on the benzene is methyl (+R effect) , the attack is from the ortho and the para positions. Para product is more stable due to less steric hinderance.

The product formed is shown in mechanism does not mention in any of the options.

So, None of these is the answer

8 0
3 years ago
Read 2 more answers
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