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NEW QUESTION: 1
EIGRP OSPF Redistribution
You are a network engineer with ROUTE.com, a small IT company. They have recently merged two organizations and now need to merge their networks as shown in the topology exhibit. One network is using OSPF as its IGP and the other is using EIGRP as its IGP. R4 has been added to the existing OSPF network to provide the interconnect between the OSPF and EIGRP networks. Two links have been added that will provide redundancy.
The network requirements state that you must be able to ping and telnet from loopback 101 on R1 to the OPSF domain test address of 172.16.1.100. All traffic must use the shortest path that provides the greatest bandwidth. The redundant paths from the OSPF network to the EIGRP network must be available in case of a link failure. No static or default routing is allowed in either network.
Previous network engineer has started the merger implementation and has successfully assigned and verified all IP addressing and basic IGP routing. You have been tasked with completing the implementation and ensuring that the network requirements are met. You may not remove or change any of the configuration commands currently on any of the routers. You may add new commands or change default values.
Answer:
Explanation:
NEW QUESTION: 2
Which command lists all tables in Gaia?
A. fw tab-s
B. fw tab-I
C. Fw tab-t
D. fw tab -list
Answer: C
NEW QUESTION: 3
A 26-year-old woman presented acutely with abdominal pain. On examination, her blood pressure was 124/72 mmHg.
Investigations:
24-h urinary dopamine10 000 nmol (<3100)
24-h urinary adrenaline43 nmol (<144)
24-h urinary noradrenaline146 nmol (<570)
CT scan of abdomen3-cm left para-aortic mass
She underwent surgical exploration and removal of the lesion, which proved to be a paraganglioma. One local lymph node, removed at the same time, was also positive for the presence of tumour.
What is the most likely underlying genetic syndrome?
A. Gardner's syndrome
B. von Hippel-Lindau syndrome
C. multiple endocrine neoplasia type 2a
D. succinate dehydrogenase type B mutation
E. neurofibromatosis type 1 mutation
Answer: D
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