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TEA [102]
2 years ago
6

Which describes funguslike protists? They are all autotrophs. They are all able to move at some point. Their pseudopods allow th

em to reproduce. Their cells do not have cell walls.
Chemistry
1 answer:
lys-0071 [83]2 years ago
3 0

Answer:

Their pseudopods allow them to reproduce.

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What is the approximate mass of one proton?
Len [333]

Answer:

One AMU or 1 Atomic Mass Unit

8 0
3 years ago
Read 2 more answers
What is the molarity of a solution that has 4.4 moles BaCl2 in 1.5 Liters of solution?
garik1379 [7]

Answer:

2.9 M

Explanation:

Step 1: Given data

Moles of barium chloride (solute): 4.4 moles

Volume of solution: 1.5 liters

Step 2: Calculate the molarity of barium chloride in the solution

The molarity is a way to quantitatively express the concentration of a solute in a solution. The molarity is equal to the moles of solute divided by the volume, in liters, of solution.

M=\frac{4.4mol}{1.5L} =2.9 M

7 0
2 years ago
What is meant by Vulcanicity?​
scZoUnD [109]

The quality or state of being volcanic.

3 0
2 years ago
The half-life of na-24 is 15 hours . when there are 1000 atoms of na-24 in a sample , a scientist starts a stopwatch . the scien
marin [14]

125 Each half life it divides by 2 the amount
1000/2=500
500/2=250
250/2=125

8 0
2 years ago
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Which statement is incorrect regarding the reaction of benzene with an electrophile? View Available Hint(s) A) The carbocation i
Leno4ka [110]

Answer:

The carbocation intermediate reacts with a nucleophile to form the addition product.

Explanation:

The reaction of benzene with an electrophile is an electrophillic substitution reaction. Here the electrophile replaces hydrogen. There is no formation of carbocation as intermediate in the reaction. Infact there is transition state where the electorphile attacks on benzene ring and at the same time the hydrogen gets removed from the benzene. So a transition carbocation is formed.

The general mechanism is shown in the figure.

i) Attack of the electrophile on the benzene (which is the nucleophile)

ii) The carbocation intermediate loses a proton from the carbon bonded to the electrophile.

iii) the carbocation formation is the rate determining step.

iv) There is no formation of addition product.

Thus the wrong statement is

The carbocation intermediate reacts with a nucleophile to form the addition product.

3 0
3 years ago
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