Answer:
Explanation:
The movement of the electrons is illustrated in the picture attached to this answer. It is a four-step reaction mechanism.
First STEP: The first step involves the transfer of an electron from sodium to form a radical anion.
Second STEP: This radical anion then removes a proton/hydrogen from ammonia in a bid to neutralize itself (hence the hydrogen becomes bonded to the anion).
Third STEP: The sodium (from NaNH₂ formed) transfers an electron again to produce a vinyl carbanion.
Fourth STEP: The carbanion then removes a proton/hydrogen from ammonia (like in the second step) to form a neutral trans-alkene.
NOTE: The circled numbers denote each step while the mechanism on the left represents the use of any alkyl group (R and R') while the mechanism on the right assumes both alkyl groups are methyl. Hence, 2-butyne started the reaction and the final product was trans-2-butene.
Ionic Equation:
H⁺(aq) + Cl⁻(aq) + Na⁺(aq) + CHO₂⁻(aq) → HCHO₂(aq) + Na⁺(aq) + Cl⁻(aq)
Net ionic equation:
H⁺(aq) + CHO₂⁻(aq) → HCHO₂(aq)
Answer:
Change in internal energy (ΔU) = -9 KJ
Explanation:
Given:
q = –8 kJ [Heat removed]
w = –1 kJ [Work done]
Find:
Change in internal energy (ΔU)
Computation:
Change in internal energy (ΔU) = q + w
Change in internal energy (ΔU) = -8 KJ + (-1 KJ)
Change in internal energy (ΔU) = -8 KJ - 1 KJ
Change in internal energy (ΔU) = -9 KJ
Answer:
we will except an increase in the polarity of the system and this will cause the Non-polar spot to be near the solvent front, while the polar spot will run at an approximate speed of 0.5 Rf
Explanation:
when we run a TLC plate in a 50/50 mixture of hexanes and ethyl acetate we will except an increase in the polarity of the system and this will cause the Non-polar spot to be near the solvent front, while the polar spot will run at an approximate speed of 0.5 Rf
The speed of the polar spot depends largely on the level of polarity, an increase in the polarity will see both spots of Neat hexane run when we run a TLC plate in a 50/50 mixture of hexanes and ethyl acetate
Answer:
K8S4O16 or K8(SO4)4 depending on if the SO4 is supposed to represent sulfate or not
Explanation:
Find the molar mass of K2SO4 first:
2K + S + 4O ≈ 174 g/mol
Divide the goal molar mass of 696 by the molar mass of the empirical formula:
696 / 174 = 4
This means you need to multiply everything in the empirical formula by 4:
K2SO4 --> K8S4O16 or K8(SO4)4 depending on if the SO4 is for sulfate or not
