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Synthetic Routes - OCR A Level Chemistry - Statistics
General Stats
- This quiz has been taken 342 times
- The average score is 11 of 15
Answer Stats
| Question | Answer | % Correct |
|---|---|---|
| What reagents do you use to go from Alkene to Alcohol? | H2O(g) / H3PO4 | 97%
|
| What reagents do you use to go from Alkene to Alkane? | H2 / Ni | 94%
|
| Haloalkane to Alcohol? | NaOH / heat | 94%
|
| What reagents for Alkane to Haloalkane? | Radical substitution: X2 / UV light | 87%
|
| Alcohol to Alkene? | H2SO4 / heat | 84%
|
| You reflux tertiary alcohol + acidified potassium dichromate What do you get? | No change | 83%
|
| Walter is doing a PAG, and needs to make methanoyl chloride from methanol. What reagents does he use? | 1. Reflux with acidified potassium dichromate THEN 2. Add SOCl2 | 76%
|
| Butan-1-ol is distilled with acidified potassium dichromate. What do you get? | Butanal | 76%
|
| Butan-2-one is reacted with Z to form an Butan-2-ol. What is Z? | NaBH4 | 76%
|
| In the last step of Walter's synthesis, he is alkylating benzene. What reagent and catalyst does he use, and what is the name of this process? | RCl / AlCl3 / Friedel-Crafts Alkylation | 64%
|
| How can you reduce a nitrile to an amine? | H2 / Ni | 61%
|
| What can Walter NOT make, in one step, using an Acyl Chloride? | Carboxylate salt, by adding NaOH | 58%
|
| NO2 to NH2? | Sn + HCl then add NaOH, to deprotonate NH3+ | 56%
|
| Walter wants to make a secondary amine from a primary amine. What reagents does he use? | CH3Cl + CH2(Cl)CH2CH(CH3)NH2 / Ethanol | 30%
|
| I am nitrating phenol What reagents do I need and what position will the substitution occur? | HNO3 only, 2 and 4 | 26%
|
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